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The AGT cytogenetics laboratory manual / / edited by Marilyn S. Arsham, Margaret J. Barch, Helen J. Lawce
| The AGT cytogenetics laboratory manual / / edited by Marilyn S. Arsham, Margaret J. Barch, Helen J. Lawce |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley-Blackwell, , 2017 |
| Descrizione fisica | 1 online resource (1,219 pages) : illustrations, tables, graphs, photographs |
| Disciplina | 611.01816 |
| Soggetto topico | Cytogenetics |
| ISBN |
1-119-06128-8
1-119-06117-2 1-119-06119-9 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
The cell and cell division / Margaret J. Barch and Helen J. Lawce -- Cytogenetics : an overview / Helen J. Lawce and Michael G. Brown -- Peripheral blood cytogenetic methods / Helen J. Lawce and Michael G. Brown -- General cell culture principles and fibroblast culture / Debra F. Saxe, Kristin M. May, Jean H. Priest -- Prenatal chromosome diagnosis / Kristin M. May, Debra F. Saxe, Jean H. Priest -- Chromosome stains / Helen J. Lawce -- Human chromosomes : identification and variations / Helen J. Lawce and Luke Boyd -- ISCN : the universal language of cytogenetics / Marilyn Schaeffer Arsham and Lisa G. Shaffer -- Constitutional chromosome abnormalities / Kathleen Kaiser-Rogers -- Genomic imprinting / R. Ellen Magenis -- Cytogenetic analysis of hematologic malignant disease / Nyla Heerema -- Cytogenetic methods and findings in human solid tumors / Marilu Nelson --
Chromosome instability syndromes / Yassmine Akkari -- Microscopy and imaging / Margaret J. Barch and Helen J. Lawce -- Computer imaging / Christine E. Haessig -- Fluorescence in situ hybridization (FISH) / Helen J. Lawce and Jeff Sanford -- Multicolor FISH (SKY and M-FISH) and CGH / Turid Knutsen -- Genomic microarray technologies for the cytogenetics laboratory / Bhavana J. Dave and Warren G. Sanger -- Mathematics for the cytogenetics technologist / Patricia K. Dowling -- Selected topics on safety, equipment maintenance, and compliance for the cytogenetics laboratory / Helen Jenks and Janet Krueger -- A system approach to quality / Peggy J. Stupca and Sheryl A. Tran -- Laboratory management / Mervat Ayad and Adam Sbeiti -- Laboratory information system / Peining Li and Richard Van Rheeden -- Animal cytogenetics / Marlys L. Houck, Teri L. Lear, Suellen J. Charter -- Online genetic resources & references / Wahab A. Khan. |
| Record Nr. | UNINA-9910270883703321 |
| Hoboken, New Jersey : , : Wiley-Blackwell, , 2017 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
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 |
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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Beyond the gene [[electronic resource] ] : cytoplasmic inheritance and the struggle for authority in genetics / / Jan Sapp
| Beyond the gene [[electronic resource] ] : cytoplasmic inheritance and the struggle for authority in genetics / / Jan Sapp |
| Autore | Sapp Jan |
| Pubbl/distr/stampa | New York, : Oxford University Press, 1987 |
| Descrizione fisica | 1 online resource (283 p.) |
| Disciplina | 575.1/09 |
| Collana | Monographs on the history and philosophy of biology |
| Soggetto topico |
Cytoplasmic inheritance
Cytogenetics |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-53325-0
9786610533251 0-19-536468-6 1-4294-0148-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Contents; Introduction; Chapter 1. Defining the Organism; Chapter 2. Constructing Heredity; Chapter 3. Challenging the Nuclear Monopoly of the Cell in Germany; Chapter 4. T. M. Sonneborn: Making Plasmagenes in America; Chapter 5. Boris Ephrussi and the Birth of Genetics in France; Chapter 6. The Cold War in Genetics; Chapter 7. Problems with ""Master Molecules""; Chapter 8. Patterns of Power; Bibliography; Index |
| Record Nr. | UNINA-9910458647003321 |
|
Sapp Jan
|
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| New York, : Oxford University Press, 1987 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Beyond the gene [[electronic resource] ] : cytoplasmic inheritance and the struggle for authority in genetics / / Jan Sapp
| Beyond the gene [[electronic resource] ] : cytoplasmic inheritance and the struggle for authority in genetics / / Jan Sapp |
| Autore | Sapp Jan |
| Pubbl/distr/stampa | New York, : Oxford University Press, 1987 |
| Descrizione fisica | 1 online resource (283 p.) |
| Disciplina | 575.1/09 |
| Collana | Monographs on the history and philosophy of biology |
| Soggetto topico |
Cytoplasmic inheritance
Cytogenetics |
| ISBN |
1-280-53325-0
9786610533251 0-19-536468-6 1-4294-0148-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Contents; Introduction; Chapter 1. Defining the Organism; Chapter 2. Constructing Heredity; Chapter 3. Challenging the Nuclear Monopoly of the Cell in Germany; Chapter 4. T. M. Sonneborn: Making Plasmagenes in America; Chapter 5. Boris Ephrussi and the Birth of Genetics in France; Chapter 6. The Cold War in Genetics; Chapter 7. Problems with ""Master Molecules""; Chapter 8. Patterns of Power; Bibliography; Index |
| Record Nr. | UNINA-9910784879603321 |
|
Sapp Jan
|
||
| New York, : Oxford University Press, 1987 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Beyond the gene : cytoplasmic inheritance and the struggle for authority in genetics / / Jan Sapp
| Beyond the gene : cytoplasmic inheritance and the struggle for authority in genetics / / Jan Sapp |
| Autore | Sapp Jan |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | New York, : Oxford University Press, 1987 |
| Descrizione fisica | 1 online resource (283 p.) |
| Disciplina | 575.1/09 |
| Collana | Monographs on the history and philosophy of biology |
| Soggetto topico |
Cytoplasmic inheritance
Cytogenetics |
| ISBN |
1-280-53325-0
9786610533251 0-19-536468-6 1-4294-0148-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Contents; Introduction; Chapter 1. Defining the Organism; Chapter 2. Constructing Heredity; Chapter 3. Challenging the Nuclear Monopoly of the Cell in Germany; Chapter 4. T. M. Sonneborn: Making Plasmagenes in America; Chapter 5. Boris Ephrussi and the Birth of Genetics in France; Chapter 6. The Cold War in Genetics; Chapter 7. Problems with ""Master Molecules""; Chapter 8. Patterns of Power; Bibliography; Index |
| Record Nr. | UNINA-9910823592003321 |
|
Sapp Jan
|
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| New York, : Oxford University Press, 1987 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Biologia molecolare del gene / James D. Watson
| Biologia molecolare del gene / James D. Watson |
| Autore | Watson, James D. |
| Edizione | [3. ed.] |
| Pubbl/distr/stampa | Bologna : Zanichelli, c1978 |
| Descrizione fisica | xii, 771 p. : ill. ; 24 cm |
| Disciplina | 572.8 |
| Soggetto topico |
Cytogenetics
Molecular biology Molecular genetics |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Record Nr. | UNISALENTO-991003431439707536 |
|
Watson, James D.
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| Bologna : Zanichelli, c1978 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. del Salento | ||
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Biologia molecolare del gene / James D. Watson ... [et al.]
| Biologia molecolare del gene / James D. Watson ... [et al.] |
| Edizione | [5. ed.] |
| Pubbl/distr/stampa | Bologna : Zanichelli, 2005 |
| Descrizione fisica | xxi, 698 p. : ill. ; 24 cm |
| Disciplina | 572.8 |
| Altri autori (Persone) |
Watson, James D.
Baker, Tania A. Bell, Stephen P. Losick, Richard Levine, Michael Gann, Alexander |
| Soggetto topico |
Cytogenetics
Molecular biology Molecular genetics |
| ISBN | 8808129357 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Record Nr. | UNISALENTO-991002104969707536 |
| Bologna : Zanichelli, 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. del Salento | ||
| ||
Biologia molecolare del gene / James D. Watson ... [et al.]
| Biologia molecolare del gene / James D. Watson ... [et al.] |
| Edizione | [4th ed.] |
| Pubbl/distr/stampa | Bologna : Zanichelli, c1989 |
| Descrizione fisica | 2 v. (xxvi, [863] p.)(xxiv, [516] p.) : ill. ; 28 cm |
| Disciplina | 572.8 |
| Altri autori (Persone) | Watson, James D. |
| Soggetto topico |
Cytogenetics
Molecular biology Molecular genetics |
| ISBN |
8808064581 (v.1)
8808119823 (v.2) |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Nota di contenuto |
V.1 : Principi generali
V.2 : Aspetti speciali |
| Record Nr. | UNISALENTO-991003431479707536 |
| Bologna : Zanichelli, c1989 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. del Salento | ||
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Cancer cytogenetics : chromosomal and molecular genetic aberrations of tumor cells / / edited by Sverre Heim, Felix Mitelman ; contributors, Sietse M. Aukema [and twenty six others]
| Cancer cytogenetics : chromosomal and molecular genetic aberrations of tumor cells / / edited by Sverre Heim, Felix Mitelman ; contributors, Sietse M. Aukema [and twenty six others] |
| Edizione | [Fourth edition.] |
| Pubbl/distr/stampa | Chichester, [England] : , : Wiley Blackwell, , 2015 |
| Descrizione fisica | 1 online resource (645 p.) |
| Disciplina | 616.994042 |
| Soggetto topico |
Cancer - Genetic aspects
Cytogenetics |
| ISBN |
1-118-79552-0
1-118-79551-2 1-118-79556-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | How it all began : cancer cytogenetics before sequencing / Felix Mitelman, Sverre Heim -- Cytogenetic methods / David Gisselsson -- Cytogenetic nomenclature / Sverre Heim, Felix Mitelman -- Nonrandom chromosome abnormalities in cancer : an overview / Sverre Heim, Felix Mitelman -- From chromosomes to genes : searching for pathogenetic fusions in cancer / Ioannis Panagopoulos -- Acute myeloid leukemia / Bertil Johansson, Christine Harrison -- Myelodysplastic syndromes / Harold J. Olney, Michelle M. Le Beau -- Chronic myeloid leukemia / Thoas Fioretos -- Chronic myeloproliferative neoplasms / Peter Vandenberghe, Lucienne Michaux -- Acute lymphoblastic leukemia / Christine Harrison, Bertil Johansson -- Mature B- and T-cell neoplasms and Hodgkin lymphoma / Reiner Siebert, Sietse M. Aukema -- Tumors of the upper aerodigestive tract / Susanne M. Gollin -- Tumors of the lung / Penny Nymark, Eeva Kettunen, Sakari Knuutila -- Tumors of the digestive tract / Georgia Bardi, Sverre Heim -- Tumors of the urinary tract / Paola Dal Cin -- Tumors of the breast / Manuel R.Teixeira, Nikos Pandis, Sverre Heim -- Tumors of the female genital system / Francesca Micci, Sverre Heim -- Tumors of the male genital organs / Manuel Teixeira, Sverre Heim -- Tumors of endocrine glands / Jörn Bullerdiek and David Gisselsson -- Tumors of the nervous system / Petter Brandal, Sverre Heim -- Tumors of the eye / Karen Sisley -- Tumors of the skin / Fredrik Mertens, Felix Mitelman, Sverre Heim -- Tumors of bone / Fredrik Mertens, Nils Mandahl -- Soft tissue tumors / Nils Mandahl, Fredrik Mertens. |
| Record Nr. | UNINA-9910131545703321 |
| Chichester, [England] : , : Wiley Blackwell, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Cancer cytogenetics : chromosomal and molecular genetic aberrations of tumor cells / / edited by Sverre Heim, Felix Mitelman ; contributors, Sietse M. Aukema [and twenty six others]
| Cancer cytogenetics : chromosomal and molecular genetic aberrations of tumor cells / / edited by Sverre Heim, Felix Mitelman ; contributors, Sietse M. Aukema [and twenty six others] |
| Edizione | [Fourth edition.] |
| Pubbl/distr/stampa | Chichester, [England] : , : Wiley Blackwell, , 2015 |
| Descrizione fisica | 1 online resource (645 p.) |
| Disciplina | 616.994042 |
| Soggetto topico |
Cancer - Genetic aspects
Cytogenetics |
| ISBN |
1-118-79552-0
1-118-79551-2 1-118-79556-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | How it all began : cancer cytogenetics before sequencing / Felix Mitelman, Sverre Heim -- Cytogenetic methods / David Gisselsson -- Cytogenetic nomenclature / Sverre Heim, Felix Mitelman -- Nonrandom chromosome abnormalities in cancer : an overview / Sverre Heim, Felix Mitelman -- From chromosomes to genes : searching for pathogenetic fusions in cancer / Ioannis Panagopoulos -- Acute myeloid leukemia / Bertil Johansson, Christine Harrison -- Myelodysplastic syndromes / Harold J. Olney, Michelle M. Le Beau -- Chronic myeloid leukemia / Thoas Fioretos -- Chronic myeloproliferative neoplasms / Peter Vandenberghe, Lucienne Michaux -- Acute lymphoblastic leukemia / Christine Harrison, Bertil Johansson -- Mature B- and T-cell neoplasms and Hodgkin lymphoma / Reiner Siebert, Sietse M. Aukema -- Tumors of the upper aerodigestive tract / Susanne M. Gollin -- Tumors of the lung / Penny Nymark, Eeva Kettunen, Sakari Knuutila -- Tumors of the digestive tract / Georgia Bardi, Sverre Heim -- Tumors of the urinary tract / Paola Dal Cin -- Tumors of the breast / Manuel R.Teixeira, Nikos Pandis, Sverre Heim -- Tumors of the female genital system / Francesca Micci, Sverre Heim -- Tumors of the male genital organs / Manuel Teixeira, Sverre Heim -- Tumors of endocrine glands / Jörn Bullerdiek and David Gisselsson -- Tumors of the nervous system / Petter Brandal, Sverre Heim -- Tumors of the eye / Karen Sisley -- Tumors of the skin / Fredrik Mertens, Felix Mitelman, Sverre Heim -- Tumors of bone / Fredrik Mertens, Nils Mandahl -- Soft tissue tumors / Nils Mandahl, Fredrik Mertens. |
| Record Nr. | UNINA-9910818268703321 |
| Chichester, [England] : , : Wiley Blackwell, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Soggetto topico
-
Cytogenetics
(88)
- Cytogénétique (15)
- Cell Biology (12)
- Cell biology (10)
- Molecular Biology (10)