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American journal of medical genetics
| American journal of medical genetics |
| Pubbl/distr/stampa | New York, : Wiley-Liss |
| Disciplina | 616/.042 |
| ISSN | 0148-7299 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Note periodicità | Bimensile |
| Record Nr. | UNINA-990008891460403321 |
| New York, : Wiley-Liss | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Aneuploidy [[electronic resource] ] : etiology, disorders and risk factors / / Salvatore de Rossi and Filippo Bianchi, editors
| Aneuploidy [[electronic resource] ] : etiology, disorders and risk factors / / Salvatore de Rossi and Filippo Bianchi, editors |
| Pubbl/distr/stampa | Hauppauge, N.Y., : Nova Science Publishers, c2012 |
| Descrizione fisica | 1 online resource (185 p.) |
| Disciplina | 616/.042 |
| Altri autori (Persone) |
De RossiSalvatore
BianchiFilippo <1964-> |
| Collana | Genetics--research and issues |
| Soggetto topico | Aneuploidy |
| Soggetto genere / forma | Electronic books. |
| ISBN | 1-62100-215-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Aneuploidy : mechanisms, cancer, and the role of environmental pollutants / Amie L. Holmes, John Pierce Wise Sr. -- Ploidy in mitosis and meiosis : a role of MAPK/Erk network / Franck Riquet, Pauline Vandame, Jean-Francois Bodart -- The spindle assembly checkpoint and aneuploidy / Juliana Faria ... [et al.] -- The role of centromere cohesion and associated proteins in Alzheimer's disease : a relation to aneuploidy? / V.P Bajic ... [et al.] -- Cohesins, genomic stability, and cancer / José L. Barbero -- Adult neurogenesis and aneuploidy in etiology, pathogenesis, and pathology of Alzheimer's disease / Philippe Taupin -- Aneuploidy in cultured human multipotent mesenchymal stromal cells / V.A. Nikitina ... [et al.] -- Somatic and germ cells spontaneous aneuploidy level in healthy fertile people / N. Zotova ... [et al.] -- Sperm aneuploidy and male fertility / El-Sayed A. Mohamed, Myung-Geol Pang -- Role of mammalian ChlR1 in chromosome segregation in mitosis / Akira Inoue. |
| Record Nr. | UNINA-9910463206403321 |
| Hauppauge, N.Y., : Nova Science Publishers, c2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Aneuploidy [[electronic resource] ] : etiology, disorders and risk factors / / Salvatore de Rossi and Filippo Bianchi, editors
| Aneuploidy [[electronic resource] ] : etiology, disorders and risk factors / / Salvatore de Rossi and Filippo Bianchi, editors |
| Pubbl/distr/stampa | Hauppauge, N.Y., : Nova Science Publishers, c2012 |
| Descrizione fisica | 1 online resource (185 p.) |
| Disciplina | 616/.042 |
| Altri autori (Persone) |
De RossiSalvatore
BianchiFilippo <1964-> |
| Collana | Genetics--research and issues |
| Soggetto topico | Aneuploidy |
| ISBN | 1-62100-215-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Aneuploidy : mechanisms, cancer, and the role of environmental pollutants / Amie L. Holmes, John Pierce Wise Sr. -- Ploidy in mitosis and meiosis : a role of MAPK/Erk network / Franck Riquet, Pauline Vandame, Jean-Francois Bodart -- The spindle assembly checkpoint and aneuploidy / Juliana Faria ... [et al.] -- The role of centromere cohesion and associated proteins in Alzheimer's disease : a relation to aneuploidy? / V.P Bajic ... [et al.] -- Cohesins, genomic stability, and cancer / José L. Barbero -- Adult neurogenesis and aneuploidy in etiology, pathogenesis, and pathology of Alzheimer's disease / Philippe Taupin -- Aneuploidy in cultured human multipotent mesenchymal stromal cells / V.A. Nikitina ... [et al.] -- Somatic and germ cells spontaneous aneuploidy level in healthy fertile people / N. Zotova ... [et al.] -- Sperm aneuploidy and male fertility / El-Sayed A. Mohamed, Myung-Geol Pang -- Role of mammalian ChlR1 in chromosome segregation in mitosis / Akira Inoue. |
| Record Nr. | UNINA-9910786862803321 |
| Hauppauge, N.Y., : Nova Science Publishers, c2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Applications of toxicogenomic technologies to predictive toxicology and risk assessment [[electronic resource] /] / Committee on Applications of Toxicogenomic Technologies to Predictive Toxicology ; Board on Environmental Studies and Toxicology ; Board on Life Studies ; Division on Earth and Life Studies ; National Research Council of the National Academies
| Applications of toxicogenomic technologies to predictive toxicology and risk assessment [[electronic resource] /] / Committee on Applications of Toxicogenomic Technologies to Predictive Toxicology ; Board on Environmental Studies and Toxicology ; Board on Life Studies ; Division on Earth and Life Studies ; National Research Council of the National Academies |
| Pubbl/distr/stampa | Washington, D.C., : National Academies Press, c2007 |
| Descrizione fisica | 1 online resource (299 p.) |
| Disciplina | 616/.042 |
| Soggetto topico |
Genetic toxicology
DNA microarrays - Statistical methods Health risk assessment Carcinogenesis |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-281-10990-8
9786611109905 0-309-11299-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910452115503321 |
| Washington, D.C., : National Academies Press, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Applications of toxicogenomic technologies to predictive toxicology and risk assessment [[electronic resource] /] / Committee on Applications of Toxicogenomic Technologies to Predictive Toxicology ; Board on Environmental Studies and Toxicology ; Board on Life Studies ; Division on Earth and Life Studies ; National Research Council of the National Academies
| Applications of toxicogenomic technologies to predictive toxicology and risk assessment [[electronic resource] /] / Committee on Applications of Toxicogenomic Technologies to Predictive Toxicology ; Board on Environmental Studies and Toxicology ; Board on Life Studies ; Division on Earth and Life Studies ; National Research Council of the National Academies |
| Pubbl/distr/stampa | Washington, D.C., : National Academies Press, c2007 |
| Descrizione fisica | 1 online resource (299 p.) |
| Disciplina | 616/.042 |
| Soggetto topico |
Genetic toxicology
DNA microarrays - Statistical methods Health risk assessment Carcinogenesis |
| ISBN |
0-309-17889-4
1-281-10990-8 9786611109905 0-309-11299-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Introduction -- Toxicogenomic technologies -- Experimental design and data analysis -- Application to exposure assessment -- Application to hazard screening -- Application to analyzing variation in human susceptibility -- Application to the study of mechanisms of action -- Other potential applications of toxicogenomic technologies to risk assessment -- Validation -- Sample and data collection and analysis -- Ethical, legal, and social issues -- Conculsions and recommendations. |
| Record Nr. | UNINA-9910778274603321 |
| Washington, D.C., : National Academies Press, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Applications of Toxicogenomics in Safety Evaluation and Risk Assessment [[electronic resource]]
| Applications of Toxicogenomics in Safety Evaluation and Risk Assessment [[electronic resource]] |
| Autore | Boverhof Darrell R |
| Pubbl/distr/stampa | Hoboken, : Wiley, 2011 |
| Descrizione fisica | 1 online resource (402 p.) |
| Disciplina |
616.042
616/.042 |
| Altri autori (Persone) | GollapudiB. Bhaskar |
| Soggetto topico |
Genetic toxicology
Health risk assessment Risk Assessment Toxicity testing Toxicogenetics Toxicology Pharmacogenetics Risk Risk Management Epidemiologic Measurements Organization and Administration Pharmacology Probability Genetics Public Health Health Occupations Statistics as Topic Biological Science Disciplines Biology Health Services Administration Environment and Public Health Natural Science Disciplines Health Care Health Care Evaluation Mechanisms Epidemiologic Methods Quality of Health Care Investigative Techniques Health Care Quality, Access, and Evaluation Health & Biological Sciences Toxicology & Public Health |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-283-23966-3
9786613239662 1-118-00104-4 1-118-00103-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Contents; Preface; Contributors; 1 Toxicology, ""Omics"" Technologies, and Toxicogenomics: A Primer; 2 Introduction to Human Health Risk Assessment; 3 Practical Considerations for the Application of Toxicogenomics to Risk Assessment: Early Experience, Current Drivers, and a Path Forward; 4 Approaches and Practical Considerations for the Analysis of Toxicogenomics Data; 5 Genomics in Identifying Mutagenic Mode of Action in Carcinogenesis; 6 Application of Genomics for Predicting and Understanding the Mode of Action for Nongenotoxic Carcinogens; 7 Genomics in Characterizing Endocrine Toxicity
8 Studying Organ-Specific Toxicity Using Gene-Expression Profiling9 Toxicogenomic Studies in Human Populations; 10 Toxicogenomics Applied to Ecological Risk Assessment; 11 Analysis of Transcriptomic Dose-Response Data for Toxicology and Risk Assessment; 12 Toxicogenomics as a Tool for Validating Animal to Human Extrapolations in Chemical Risk Assessment: Concepts, Applications, and Challenges; 13 Toxicogenomics and Animal Alternatives; 14 Toxicogenomics and the Regulatory Framework; 15 Standardization of Gene-Expression Information for the Safety Evaluation: Activities in Japan 16 Applying Transcriptional Profiling in Drug Safety Evaluation17 Reframing the Risk Assessment Paradigm: Toward a Systems Biology Approach; Index |
| Record Nr. | UNINA-9910139607903321 |
Boverhof Darrell R
|
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| Hoboken, : Wiley, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Applications of Toxicogenomics in Safety Evaluation and Risk Assessment
| Applications of Toxicogenomics in Safety Evaluation and Risk Assessment |
| Autore | Boverhof Darrell R |
| Edizione | [First edition.] |
| Pubbl/distr/stampa | Hoboken : , : Wiley, , 2011 |
| Descrizione fisica | 1 online resource (402 pages) |
| Disciplina |
616.042
616/.042 |
| Altri autori (Persone) | GollapudiB. Bhaskar |
| Soggetto topico |
Genetic toxicology
Health risk assessment Risk Assessment Toxicity testing Toxicogenetics Toxicology Pharmacogenetics Risk Risk Management Epidemiologic Measurements Organization and Administration Pharmacology Probability Genetics Public Health Health Occupations Statistics as Topic Biological Science Disciplines Biology Health Services Administration Environment and Public Health Natural Science Disciplines Delivery of Health Care Health Care Evaluation Mechanisms Epidemiologic Methods Quality of Health Care Investigative Techniques Health Care Quality, Access, and Evaluation Health & Biological Sciences Toxicology & Public Health |
| ISBN |
1-283-23966-3
9786613239662 1-118-00104-4 1-118-00103-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Contents; Preface; Contributors; 1 Toxicology, ""Omics"" Technologies, and Toxicogenomics: A Primer; 2 Introduction to Human Health Risk Assessment; 3 Practical Considerations for the Application of Toxicogenomics to Risk Assessment: Early Experience, Current Drivers, and a Path Forward; 4 Approaches and Practical Considerations for the Analysis of Toxicogenomics Data; 5 Genomics in Identifying Mutagenic Mode of Action in Carcinogenesis; 6 Application of Genomics for Predicting and Understanding the Mode of Action for Nongenotoxic Carcinogens; 7 Genomics in Characterizing Endocrine Toxicity
8 Studying Organ-Specific Toxicity Using Gene-Expression Profiling9 Toxicogenomic Studies in Human Populations; 10 Toxicogenomics Applied to Ecological Risk Assessment; 11 Analysis of Transcriptomic Dose-Response Data for Toxicology and Risk Assessment; 12 Toxicogenomics as a Tool for Validating Animal to Human Extrapolations in Chemical Risk Assessment: Concepts, Applications, and Challenges; 13 Toxicogenomics and Animal Alternatives; 14 Toxicogenomics and the Regulatory Framework; 15 Standardization of Gene-Expression Information for the Safety Evaluation: Activities in Japan 16 Applying Transcriptional Profiling in Drug Safety Evaluation17 Reframing the Risk Assessment Paradigm: Toward a Systems Biology Approach; Index |
| Record Nr. | UNINA-9910824275603321 |
|
Boverhof Darrell R
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| Hoboken : , : Wiley, , 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Assessing genetic risks [[electronic resource] ] : implications for health and social policy / / Lori B. Andrews ... [et al.], editors
| Assessing genetic risks [[electronic resource] ] : implications for health and social policy / / Lori B. Andrews ... [et al.], editors |
| Pubbl/distr/stampa | Washington, D.C., : National Academy Press, 1994 |
| Descrizione fisica | xiv, 338 p. : ill |
| Disciplina | 616/.042 |
| Altri autori (Persone) | AndrewsLori B. <1952-> |
| Soggetto topico |
Medical genetics - Social aspects
Human chromosome abnormalities - Diagnosis - Social aspects Medical policy - United States |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-19640-8
9786610196401 0-309-58505-8 0-585-00217-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910455912203321 |
| Washington, D.C., : National Academy Press, 1994 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Assessing genetic risks : implications for health and social policy / / editors, Lori B. Andrews [et al.]
| Assessing genetic risks : implications for health and social policy / / editors, Lori B. Andrews [et al.] |
| Pubbl/distr/stampa | Washington, D.C. : , : National Academy Press, , 1994 |
| Descrizione fisica | xiv, 338 pages : illustrations |
| Disciplina | 616/.042 |
| Altri autori (Persone) | AndrewsLori B. <1952-> |
| Soggetto topico |
Medical genetics - Social aspects
Human chromosome abnormalities - Diagnosis - Social aspects Medical policy - United States |
| ISBN |
1-280-19640-8
9786610196401 0-309-58505-8 0-585-00217-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910778795003321 |
| Washington, D.C. : , : National Academy Press, , 1994 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Atlas of Genetic Diagnosis and Counseling [[electronic resource] /] / by Harold Chen
| Atlas of Genetic Diagnosis and Counseling [[electronic resource] /] / by Harold Chen |
| Autore | Chen Harold |
| Edizione | [2nd ed. 2012.] |
| Pubbl/distr/stampa | New York, NY : , : Springer New York : , : Imprint : Springer, , 2012 |
| Descrizione fisica | 1 online resource (2472 illus., 2018 illus. in color. eReference.) |
| Disciplina | 616/.042 |
| Soggetto topico |
Human genetics
Cytogenetics Molecular biology Pathology Human Genetics Molecular Medicine |
| ISBN | 1-4614-1037-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Acardia -- Achondrogenesis -- Achondroplasia -- Adams-Oliver syndrome -- Agnathia -- Aicardi syndrome -- Alagille syndrome -- Albinism -- Alpha thalassemia-mental retardation (ATR-X) syndrome -- Ambiguous genitalia -- Amniotic deformity, adhesions, mutilations (ADAM) syndrome -- Androgen insensitivity syndrome -- Angelman syndrome -- Apert syndrome -- Aplasia cutis congenita -- Arthrogryposis multiplex congenita -- Asphyxiating thoracic dystrophy -- Ataxia telangiectasia -- Atelosteogenesis -- Autism -- Bannayan-Riley-Ruvalcaba syndrome -- Beckwith-Wiedemann syndrome -- Behcet disease -- Biotinidase deficiency -- Bladder exstrophy -- Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) -- Body stalk anomaly -- Brachydactyly -- Branchial cleft cyst -- Calcinosis cutis -- Campomelic dysplasia -- Carpenter syndrome -- Cat-eye syndrome -- Celiac disease -- Cerebral palsy -- Cerebro-costo-mandibular syndrome -- Charcot-Marie-Tooth disease -- CHARGE association -- Cherubism -- Chiari malformation -- Chondrodysplasia punctata -- Chromosome abnormalities in pediatric solid tumors -- Cleft lip/palate -- Cleidocranial dysplasia -- Cloacal exstrophy -- Clubfoot (talipes equinovarus) -- Collodion baby -- Congenital adrenal hyperplasia -- Congenital cutis laxa -- Congenital cytomegalovirus infection -- Congenital generalized lipodystrophy -- Congenital hemihyperplasia (congenital hemihypertrophy) -- Congenital hydrocephalus -- Congenital hypothyroidism -- Congenital muscular dystrophy -- Congenital toxoplasmosis -- Conjoined twins -- Corpus-callosum agenesis/dysgenesis -- Craniometaphyseal dysplasia -- Cri-du-chat syndrome -- Crouzon syndrome -- Cutis marmorata telangiectatica congenita -- Cystic fibrosis -- Dandy-Walker malformation -- De Lange syndrome -- Del(18p) syndrome -- Del(22q11.2) syndrome -- Del(Yq) syndrome -- Diabetic embryopathy -- Down syndrome -- Duncan syndrome (X-linked lymphoproliferative disease) -- Dyschondrosteosis/Langer mesomelic dysplasia -- Dysmelia (limb deficiency/reduction) -- Dysplasia epiphysealis hemimelica -- Dystonia -- Dystrophinopathies -- EEC syndrome -- Ehlers-Danlos syndrome -- Ellis-van Creveld syndrome -- Enchondromatosis -- Epidermolysis bullosa -- Epidermolytic palmoplantar keratoderma -- Faciogenital (Aarskog) syndrome -- Facioscapulohumeral muscular dystrophy (FSH) -- Familial adenomatous polyposis syndrome -- Familial hyperlysinemia -- Familial Mediterranean fever -- Fanconi anemia -- Femoral hypoplasia-unusual facies syndrome -- Fetal akinesia syndrome -- Fetal alcohol syndrome -- Fetal hydantoin syndrome -- Fibrodysplasia ossificans progressiva -- Finlay-Marks syndrome -- Floppy infant -- Fragile X syndrome -- Fraser syndrome -- Freeman-Sheldon (whistling face) syndrome -- Friedreich ataxia -- Frontonasal dysplasia -- Galactosemia -- Gastroschisis -- Gaucher disease -- Generalized arterial calcification -- Genitopatellar syndrome -- Giant congenital melanocytic nevi (giant congenital nevi) -- Glucose-6-phosphate dehydrogenase deficiency -- Glycogen storage disease, type II (Pompe) -- Goldenhar syndrome -- Gorlin (nevoid basal cell carcinoma) syndrome -- Greig cephalopolysyndactyly syndrome -- Hallermann-Streiff syndrome -- Harlequin fetus -- Hemophilia A -- Hereditary hearing loss -- Hereditary hemochromatosis -- Hereditary multiple exostosis -- Herlyn-Werner-Wunderlich syndrome -- Holoprosencephaly -- Holt-Oram syndrome -- Huntington disease -- Hydrolethalus syndrome -- Hydrops fetalis -- Hyper-IgE syndrome -- Hypochondroplasia -- Hypoglossia-hypodactyly (oromandibular limb hypogenesis) syndrome -- Hypohidrotic ectodermal dysplasia -- Hypomelanosis of Ito -- Hypophosphatasia -- Hypopituitarism -- I(1p),I(1q) syndrome -- Isodic(Yq) syndrome -- Incontinentia pigmenti -- Infantile myofibromatosis -- Ivemark syndrome -- Jarcho-Levin syndrome -- Joubert syndrome -- Kabuki syndrome -- Kassback-Merritt syndrome -- KID syndrome -- Klinefelter syndrome -- Klippel-Feil syndrome -- Klippel-Trenaunay syndrome -- Kniest dysplasia -- Larsen syndrome -- LEOPARD syndrome -- Lesch-Nyhan syndrome -- Lethal multiple pterygium syndrome -- Loeys-Dietz syndrome -- Lowe syndrome -- Marfan syndrome -- McCune-Albright syndrome -- Meckel-Gruber syndrome -- Megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease) -- Menkes disease -- Metachromatic leukodystrophy -- Miller-Dieker syndrome -- Mitochondrial Leber hereditary optic neuropathy -- Mobius syndrome -- Mowat-Wilson Disease -- Mucolipidosis II (I-cell disease) -- Mucolipidosis III (pseudo-Hurler Polydystrophy) -- MPS I (Hurler syndrome) -- MPS II (Hunter syndrome) -- MPS III (Sanfilippo syndrome) -- MPS IV (Morquio syndrome) -- MPS VI (Maroteaux-Lamy syndrome) -- Multiple endocrine neoplasia Syndrome -- Multiple epiphyseal dysplasia -- Multiple pterygium syndrome -- Myotonic dystrophy -- Nail-Patella Syndrome (hereditary Osteo-onychodysplasia) -- Neonatal Herpes simplex infection -- Nephrogenic diabetes insipidus -- Netherton syndrome -- Neu-Laxova syndrome -- Neural tube defects -- Neurofibromatosis 1 -- Neurofibromatosis 2 -- Noonan syndrome -- Oblique facial cleft syndrome -- Oligohydramnios sequence -- Omphalocele -- Oro-Facial-Digital Syndrome -- Osteogenesis imperfecta -- Osteopetrosis -- Osteopoikilosis -- Otopalatodigital spectrum disorders -- Pachyonychia congenita -- Pallister-Killian syndrome -- Phenylketonuria (PKU) -- Pierre Robin sequence -- Polycystic kidney disease, AD form -- Polycystic kidney disease, AR form -- Popliteal pterygium syndrome -- Prader-Willi syndrome -- Progeria -- Prune belly syndrome -- Pseudoachondroplasia -- R(18) syndrome -- Retinoid embryopathy -- Rett syndrome -- Rickets -- Rigid spine syndrome -- Roberts syndrome -- Robinow syndrome -- Rubinstein-Taybi syndrome -- Saethre-Chotzen syndrome -- Sagittal synostosis associated with chromosome abnormalities -- Schizencephaly -- Schmid metaphyseal chondrodystrophy -- Seckel syndrome -- Severe combined immune deficiency -- Short rib polydactyly syndromes (SRPS) -- Sickle cell disease -- Silver-Russell syndrome -- Sirenomelia -- Smith-Lemli-Optiz syndrome -- Smith-Magenis syndrome -- Sotos syndrome -- Spinal muscular atrophy -- Spondyloepiphyseal dysplasia -- Stickler syndrome -- Sturge-Weber syndrome -- Tay-Sachs disease -- Tetrasomy 9p syndrome -- Thalassemia -- Thanatophoric dysplasia -- Thrombocytopenia-absent radius (TAR) syndrome -- Treacher-Collins syndrome -- Trimethylaminuria -- Triploidy -- Trismus pseudocamptodactyly (Hecht syndrome) -- Trisomy 8 mosaicism (Warkany) syndrome -- Trisomy 13 syndrome -- Trisomy 18 syndrome -- Tuberous sclerosis -- Turner syndrome -- Twin-twin transfusion syndrome -- Ulnar-mammary syndrome -- Urofacial (Ochoa) Syndrome -- VATER (VACTERL) association -- Von Hippel-Lindau disease -- Waardenburg syndrome -- Weill-Marchesani syndrome -- Williams syndrome -- Wolf-Hirschhorn syndrome -- X-linked agammaglobulinemia (Bruton type) -- X-linked ichthyosis -- XX Male -- XXX syndrome -- XXXXX syndrome -- XXXXY syndrome -- XY female.-XYY syndrome. |
| Record Nr. | UNINA-9910483792303321 |
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Chen Harold
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| New York, NY : , : Springer New York : , : Imprint : Springer, , 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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