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2n pollen formation : 40 cytological mechanisms of nuclear meiotic restitution / / Nataliya V. Shamina
| 2n pollen formation : 40 cytological mechanisms of nuclear meiotic restitution / / Nataliya V. Shamina |
| Autore | Shamina Nataliya V. |
| Pubbl/distr/stampa | Hauppauge, New York : , : Nova Science Publishers, , [2010] |
| Descrizione fisica | 1 online resource (121 pages) : illustrations |
| Disciplina | 571.8/452 |
| Collana | Botanical research and practices |
| Soggetto topico |
Plant cytogenetics
Chromosome abnormalities Pollen Meiosis |
| ISBN | 1-61728-804-7 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Prophase abnormalities as the reason for meiotic restitution -- Early prometaphase abnormalities leading to nuclear restitution -- Prometaphase abnormalities and meiotic restitution -- Abnormalities of late prometaphase as a meiotic restitution mechanism -- Anaphase abnormalities that lead to meiotic restitution -- Cytoskeleton abnormalities at telophase and meiotic restitution -- Cell plate abnormalities leading to meiotic restitution -- Incomplete cytokinesis as incisions on the mother cell membrane and its consequences -- General meiotic abnormalities leading to restitution discussion. |
| Altri titoli varianti | Two n pollen formation |
| Record Nr. | UNINA-9910148726603321 |
Shamina Nataliya V.
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| Hauppauge, New York : , : Nova Science Publishers, , [2010] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Abnormal chromosomes : the past, present, and future of cancer cytogenetics / / Sverre Heim, Felix Mitelman
| Abnormal chromosomes : the past, present, and future of cancer cytogenetics / / Sverre Heim, Felix Mitelman |
| Autore | Heim Sverre |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley-Blackwell, , [2022] |
| Descrizione fisica | 1 online resource (211 pages) |
| Disciplina | 616.994042 |
| Soggetto topico | Chromosome abnormalities |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-119-65203-0
1-119-65204-9 1-119-65205-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910555133403321 |
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Heim Sverre
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| Hoboken, New Jersey : , : Wiley-Blackwell, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Abnormal chromosomes : the past, present, and future of cancer cytogenetics / / Sverre Heim, Felix Mitelman
| Abnormal chromosomes : the past, present, and future of cancer cytogenetics / / Sverre Heim, Felix Mitelman |
| Autore | Heim Sverre |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley-Blackwell, , [2022] |
| Descrizione fisica | 1 online resource (211 pages) |
| Disciplina | 616.994042 |
| Soggetto topico | Chromosome abnormalities |
| ISBN |
1-119-65203-0
1-119-65204-9 1-119-65205-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910831194203321 |
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Heim Sverre
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| Hoboken, New Jersey : , : Wiley-Blackwell, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Chromosomal Abnormalities / / Tülay Askin Çelik, Subrata Dey, editors
| Chromosomal Abnormalities / / Tülay Askin Çelik, Subrata Dey, editors |
| Pubbl/distr/stampa | London : , : IntechOpen, , 2020 |
| Descrizione fisica | 1 online resource (166 pages) |
| Disciplina | 616.042 |
| Soggetto topico | Chromosome abnormalities |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910688439703321 |
| London : , : IntechOpen, , 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Chromosome abnormalities and genetic counseling [[electronic resource] /] / R.J. McKinlay Gardner, Grant R. Sutherland, Lisa G. Shaffer
| Chromosome abnormalities and genetic counseling [[electronic resource] /] / R.J. McKinlay Gardner, Grant R. Sutherland, Lisa G. Shaffer |
| Autore | Gardner R. J. M |
| Edizione | [4th ed.] |
| Pubbl/distr/stampa | Oxford, : Oxford University Press, c2012 |
| Descrizione fisica | 1 online resource (649 p.) |
| Disciplina | 616/.042 |
| Altri autori (Persone) |
SutherlandGrant R
ShafferLisa G |
| Collana | Oxford monographs on medical genetics |
| Soggetto topico |
Genetic counseling
Human chromosome abnormalities - Patients - Counseling of Chromosome abnormalities |
| Soggetto genere / forma | Electronic books. |
| ISBN |
0-19-997517-5
1-283-42706-0 9786613427069 0-19-974915-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Contents; PART ONE: BASIC CONCEPTS; 1. Elements of Medical Cytogenetics; 2. Chromosome Analysis; 3. The Origins and Consequences of Chromosome Pathology; 4. Deriving and Using a Risk Figure; PART TWO: PARENT WITH A CHROMOSOMAL ABNORMALITY; 5. Autosomal Reciprocal Translocations; 6. Sex Chromosome Translocations; 7. Robertsonian Translocations; 8. Centromere Fissions, Complementary Isochromosomes, Telomeric Fusions, Balancing Supernumerary Chromosomes, and Jumping Translocations; 9. Inversions; 10. Insertions; 11. Autosomal Ring Chromosomes; 12. Complex Rearrangements
13. Parental Sex Chromosome Aneuploidy14. Parental Autosomal Aneuploidy; 15. The Fragile X Syndromes; PART THREE: VARIANTS; 16. Variant Chromosomes and Abnormalities of No Phenotypic Consequence; 17. Copy Number Changes; PART FOUR: NORMAL PARENTS WITH A CHROMOSOMALLY ABNORMAL CHILD; 18. Down Syndrome, Other Full Aneuploidies, and Polyploidy; 19. Structural Rearrangements; 20. Chromosomal Disorders of Sex Development; 21. Chromosome Instability Syndromes; PART FIVE: DISORDERS ASSOCIATED WITH ABERRANT GENOMIC IMPRINTING; 22. Uniparental Disomy and Disorders of Imprinting PART SIX: REPRODUCTIVE FAILURE23. Gametogenesis and Conception, Pregnancy Loss and Infertility; PART SEVEN: PRENATAL DIAGNOSIS; 24. Parental Age Counseling and Screening for Fetal Trisomy; 25. Prenatal Diagnostic Procedures; 26. Preimplantation Genetic Diagnosis; 27. Chromosome Abnormalities Detected at Prenatal Diagnosis; PART EIGHT: NOXIOUS AGENTS; 28. Gonadal Cytogenetic Damage from Exposure to Extrinsic Agents; APPENDIXES; A. Ideograms of Human Chromosomes, and Haploid Autosomal Lengths; B. Cytogenetic Abbreviations and Nomenclature C. Determining 95 Percent Confidence Limits, and the Standard ErrorReferences; Index; A; B; C; D; E; F; G; H; I; J; K; L; M; N; O; P; Q; R; S; T; U; V; W; X; Y; Z |
| Record Nr. | UNINA-9910457763203321 |
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Gardner R. J. M
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| Oxford, : Oxford University Press, c2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Chromosome abnormalities and genetic counseling [[electronic resource] /] / R.J. McKinlay Gardner, Grant R. Sutherland, Lisa G. Shaffer
| Chromosome abnormalities and genetic counseling [[electronic resource] /] / R.J. McKinlay Gardner, Grant R. Sutherland, Lisa G. Shaffer |
| Autore | Gardner R. J. M |
| Edizione | [4th ed.] |
| Pubbl/distr/stampa | Oxford, : Oxford University Press, c2012 |
| Descrizione fisica | 1 online resource (649 p.) |
| Disciplina | 616/.042 |
| Altri autori (Persone) |
SutherlandGrant R
ShafferLisa G |
| Collana | Oxford monographs on medical genetics |
| Soggetto topico |
Genetic counseling
Human chromosome abnormalities - Patients - Counseling of Chromosome abnormalities |
| ISBN |
0-19-997517-5
1-283-42706-0 9786613427069 0-19-974915-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Contents; PART ONE: BASIC CONCEPTS; 1. Elements of Medical Cytogenetics; 2. Chromosome Analysis; 3. The Origins and Consequences of Chromosome Pathology; 4. Deriving and Using a Risk Figure; PART TWO: PARENT WITH A CHROMOSOMAL ABNORMALITY; 5. Autosomal Reciprocal Translocations; 6. Sex Chromosome Translocations; 7. Robertsonian Translocations; 8. Centromere Fissions, Complementary Isochromosomes, Telomeric Fusions, Balancing Supernumerary Chromosomes, and Jumping Translocations; 9. Inversions; 10. Insertions; 11. Autosomal Ring Chromosomes; 12. Complex Rearrangements
13. Parental Sex Chromosome Aneuploidy14. Parental Autosomal Aneuploidy; 15. The Fragile X Syndromes; PART THREE: VARIANTS; 16. Variant Chromosomes and Abnormalities of No Phenotypic Consequence; 17. Copy Number Changes; PART FOUR: NORMAL PARENTS WITH A CHROMOSOMALLY ABNORMAL CHILD; 18. Down Syndrome, Other Full Aneuploidies, and Polyploidy; 19. Structural Rearrangements; 20. Chromosomal Disorders of Sex Development; 21. Chromosome Instability Syndromes; PART FIVE: DISORDERS ASSOCIATED WITH ABERRANT GENOMIC IMPRINTING; 22. Uniparental Disomy and Disorders of Imprinting PART SIX: REPRODUCTIVE FAILURE23. Gametogenesis and Conception, Pregnancy Loss and Infertility; PART SEVEN: PRENATAL DIAGNOSIS; 24. Parental Age Counseling and Screening for Fetal Trisomy; 25. Prenatal Diagnostic Procedures; 26. Preimplantation Genetic Diagnosis; 27. Chromosome Abnormalities Detected at Prenatal Diagnosis; PART EIGHT: NOXIOUS AGENTS; 28. Gonadal Cytogenetic Damage from Exposure to Extrinsic Agents; APPENDIXES; A. Ideograms of Human Chromosomes, and Haploid Autosomal Lengths; B. Cytogenetic Abbreviations and Nomenclature C. Determining 95 Percent Confidence Limits, and the Standard ErrorReferences; Index; A; B; C; D; E; F; G; H; I; J; K; L; M; N; O; P; Q; R; S; T; U; V; W; X; Y; Z |
| Record Nr. | UNINA-9910781939103321 |
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Gardner R. J. M
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| Oxford, : Oxford University Press, c2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Chromosome abnormalities and genetic counseling / / R.J. McKinlay Gardner, Grant R. Sutherland, Lisa G. Shaffer
| Chromosome abnormalities and genetic counseling / / R.J. McKinlay Gardner, Grant R. Sutherland, Lisa G. Shaffer |
| Autore | Gardner R. J. M |
| Edizione | [4th ed.] |
| Pubbl/distr/stampa | Oxford, : Oxford University Press, c2012 |
| Descrizione fisica | 1 online resource (649 p.) |
| Disciplina | 616/.042 |
| Altri autori (Persone) |
SutherlandGrant R
ShafferLisa G |
| Collana | Oxford monographs on medical genetics |
| Soggetto topico |
Genetic counseling
Human chromosome abnormalities - Patients - Counseling of Chromosome abnormalities |
| ISBN |
0-19-997517-5
1-283-42706-0 9786613427069 0-19-974915-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Contents; PART ONE: BASIC CONCEPTS; 1. Elements of Medical Cytogenetics; 2. Chromosome Analysis; 3. The Origins and Consequences of Chromosome Pathology; 4. Deriving and Using a Risk Figure; PART TWO: PARENT WITH A CHROMOSOMAL ABNORMALITY; 5. Autosomal Reciprocal Translocations; 6. Sex Chromosome Translocations; 7. Robertsonian Translocations; 8. Centromere Fissions, Complementary Isochromosomes, Telomeric Fusions, Balancing Supernumerary Chromosomes, and Jumping Translocations; 9. Inversions; 10. Insertions; 11. Autosomal Ring Chromosomes; 12. Complex Rearrangements
13. Parental Sex Chromosome Aneuploidy14. Parental Autosomal Aneuploidy; 15. The Fragile X Syndromes; PART THREE: VARIANTS; 16. Variant Chromosomes and Abnormalities of No Phenotypic Consequence; 17. Copy Number Changes; PART FOUR: NORMAL PARENTS WITH A CHROMOSOMALLY ABNORMAL CHILD; 18. Down Syndrome, Other Full Aneuploidies, and Polyploidy; 19. Structural Rearrangements; 20. Chromosomal Disorders of Sex Development; 21. Chromosome Instability Syndromes; PART FIVE: DISORDERS ASSOCIATED WITH ABERRANT GENOMIC IMPRINTING; 22. Uniparental Disomy and Disorders of Imprinting PART SIX: REPRODUCTIVE FAILURE23. Gametogenesis and Conception, Pregnancy Loss and Infertility; PART SEVEN: PRENATAL DIAGNOSIS; 24. Parental Age Counseling and Screening for Fetal Trisomy; 25. Prenatal Diagnostic Procedures; 26. Preimplantation Genetic Diagnosis; 27. Chromosome Abnormalities Detected at Prenatal Diagnosis; PART EIGHT: NOXIOUS AGENTS; 28. Gonadal Cytogenetic Damage from Exposure to Extrinsic Agents; APPENDIXES; A. Ideograms of Human Chromosomes, and Haploid Autosomal Lengths; B. Cytogenetic Abbreviations and Nomenclature C. Determining 95 Percent Confidence Limits, and the Standard ErrorReferences; Index; A; B; C; D; E; F; G; H; I; J; K; L; M; N; O; P; Q; R; S; T; U; V; W; X; Y; Z |
| Record Nr. | UNINA-9910827819003321 |
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Gardner R. J. M
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| Oxford, : Oxford University Press, c2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Genes, chromosomes & cancer
| Genes, chromosomes & cancer |
| Pubbl/distr/stampa | [New York, N.Y.], : Wiley-Liss, Inc |
| Disciplina | 616 |
| Soggetto topico |
Cancer - Genetic aspects
Chromosome abnormalities Cell Transformation, Neoplastic Chromosome Aberrations Cancer - Aspect génétique Aberrations chromosomiques |
| Soggetto genere / forma |
Periodical
Periodicals. Périodiques. |
| ISSN | 1098-2264 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Genes, chromosomes, and cancer |
| Record Nr. | UNINA-9910154557403321 |
| [New York, N.Y.], : Wiley-Liss, Inc | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Genes, chromosomes & cancer
| Genes, chromosomes & cancer |
| Pubbl/distr/stampa | [New York, N.Y.], : Wiley-Liss, Inc |
| Disciplina | 616 |
| Soggetto topico |
Cancer - Genetic aspects
Chromosome abnormalities Cell Transformation, Neoplastic Chromosome Aberrations Cancer - Aspect génétique Aberrations chromosomiques |
| Soggetto genere / forma |
Periodical
Periodicals. Périodiques. |
| ISSN | 1098-2264 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Genes, chromosomes, and cancer |
| Record Nr. | UNISA-996216246903316 |
| [New York, N.Y.], : Wiley-Liss, Inc | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Medical genetics at a glance [[electronic resource] /] / Dorian J. Pritchard, Bruce R. Korf
| Medical genetics at a glance [[electronic resource] /] / Dorian J. Pritchard, Bruce R. Korf |
| Autore | Pritchard D. J (Dorian J.) |
| Edizione | [3rd ed.] |
| Pubbl/distr/stampa | Chichester, England, : Wiley-Blackwell, c2013 |
| Descrizione fisica | 1 online resource (233 p.) |
| Disciplina | 616/.042 |
| Altri autori (Persone) | KorfBruce R |
| Collana | At a Glance |
| Soggetto topico |
Genetic disorders
Chromosome abnormalities Medical genetics |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-118-68900-3
1-118-68902-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title page; Copyright page; Contents; Preface to the first edition; Preface to the third edition; Acknowledgements; List of abbreviations; Part 1 : Overview; 1: The place of genetics in medicine; The case for genetics; Genes in development; Genotype and phenotype; Genetics in medicine; The application of genetics; Part 2 : The Mendelian approach; 2: Pedigree drawing; Overview; The medical history; Rules for pedigree diagrams; The practical approach; Use of pedigrees; 3: Mendel's laws; Overview; The principle of unit inheritance; The principle of dominance; The principle of segregation
Example The principle of independent assortment; Example; The test-mating; Matings between double heterozygotes; Biological support for Mendel's laws; Exceptions to Mendel's laws; 1. Sex-related effects; 2. Mitochondrial inheritance; 3. Genetic linkage; 4. Polygenic conditions; 5. Overdominance, codominance, variable expressivity and incomplete penetrance; 6. Genomic imprinting; 7. Dynamic mutation; 8. Meiotic drive; Conclusion; 4: Principles of autosomal dominant inheritance and pharmacogenetics; Overview; Rules for autosomal dominant inheritance; Example; Estimation of risk Estimation of mutation rate Pharmacogenetics; Debrisoquine hydroxylase deficiency (AR); Porphyria variegata (AD); G6PD deficiency (X-linked R) (see Chapter 11); N-acetyl transferase deficiency (AR); Pseudocholinesterase deficiency (AR); Halothane sensitivity, malignant hyperthermia (genetically heterogeneous); Thiopurine methyltransferase deficiency (ACo-D); 5: Autosomal dominant inheritance, clinical examples; Overview; Disorders of the fibroblast growth factor receptors; Achondroplasia; Marfan syndrome (MFS); Familial hypercholesterolaemia (FH); Dentinogenesis imperfecta 1 (DGI) Otosclerosis 1 (OTSC1)Adult polycystic kidney disease (APKD, PKD); Multiple hereditary exostoses (EXT); 6: Autosomal recessive inheritance, principles; Overview; Rules for autosomal recessive inheritance; Example: albinism; Estimation of risk; Example: congenital deafness; 7: Consanguinity and major disabling autosomal recessive conditions; Overview; Management issues; Consanguineous matings; Incestuous matings; Brother-sister matings; Parent-child matings; Risk for offspring; First cousin marriages; Mental handicap; Oculocutaneous albinism; Recessive blindness; Retinitis pigmentosa (RP) Severe congenital deafness Connexin 26 defects (CX26); Pendred syndrome (PDS); 8: Autosomal recessive inheritance, life-threatening conditions; Overview; Cystic fibrosis (CF); Tay-Sachs disease, GM2 gangliosidosis; Phenylketonuria (PKU); Spinal muscular atrophy (SMA); 9: Aspects of dominance; Overview; Codominance (Co-D), the ABO blood groups; Incomplete dominance, overdominance and heterosis; Incomplete penetrance; Delayed onset; Variable expressivity; Neurofibromatosis type 1 (NF1), Von Recklinghausen disease; 10: X-linked and Y-linked inheritance; Overview Rules of X-linked recessive inheritance |
| Record Nr. | UNINA-9910452185503321 |
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Pritchard D. J (Dorian J.)
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| Chichester, England, : Wiley-Blackwell, c2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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