An atlas of Drosophila genes [[electronic resource]] |
Autore | Maroni Gustavo |
Pubbl/distr/stampa | New York ; , : Oxford University Press, , 2023 |
Descrizione fisica | x, 415 p. : ill |
Disciplina | 595.77/4 |
Collana | Oxford scholarship online |
Soggetto topico | Drosophila - Genome mapping |
ISBN |
0-19-770026-8
0-19-802352-9 9786610525911 1-4294-0113-3 1-280-52591-6 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910822576303321 |
Maroni Gustavo
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New York ; , : Oxford University Press, , 2023 | ||
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Lo trovi qui: Univ. Federico II | ||
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An atlas of Drosophila genes [[electronic resource] ] : sequences and molecular features / / Gustavo Maroni with contributions by Stephen M. Mount ... [et al.] |
Autore | Maroni Gustavo |
Pubbl/distr/stampa | New York, : Oxford University Press, 1993 |
Descrizione fisica | 1 online resource (428 p.) |
Disciplina | 595.77/4 |
Soggetto topico |
Drosophila - Genetics
Gene mapping |
Soggetto genere / forma | Electronic books. |
ISBN |
1-280-52591-6
9786610525911 0-19-802352-9 1-4294-0113-3 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Contents; I; II; Appendix; Index |
Record Nr. | UNINA-9910452062003321 |
Maroni Gustavo
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New York, : Oxford University Press, 1993 | ||
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Lo trovi qui: Univ. Federico II | ||
|
An atlas of Drosophila genes [[electronic resource] ] : sequences and molecular features / / Gustavo Maroni with contributions by Stephen M. Mount ... [et al.] |
Autore | Maroni Gustavo |
Pubbl/distr/stampa | New York, : Oxford University Press, 1993 |
Descrizione fisica | x, 415 p. : ill |
Disciplina | 595.77/4 |
Soggetto topico |
Drosophila - Genetics
Gene mapping |
ISBN |
0-19-770026-8
0-19-802352-9 9786610525911 1-4294-0113-3 1-280-52591-6 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910795862503321 |
Maroni Gustavo
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||
New York, : Oxford University Press, 1993 | ||
![]() | ||
Lo trovi qui: Univ. Federico II | ||
|
Molecular and genetic analysis of human traits [[electronic resource] /] / Gustavo Maroni |
Autore | Maroni Gustavo |
Pubbl/distr/stampa | Malden, MA, : Blackwell Science, c2001 |
Descrizione fisica | 1 online resource (296 p.) |
Disciplina | 599.935 |
Soggetto topico |
Human genetics
Medical genetics |
Soggetto genere / forma | Electronic books. |
ISBN |
1-281-32161-3
9786611321611 0-470-76007-9 0-470-75980-1 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Contents; PREFACE; CHAPTER 1 The Inheritance of Simple Mendelian Traits in Humans; DETECTING MENDELIAN INHERITANCE IN HUMANS; Test-Crosses and Pure Lines versus Pedigrees and Inferred Genotypes; Box 1.1 Early observations of Mendelian inheritance in humans; PATTERNS OF INHERITANCE AND EXAMPLES; Autosomal Dominant Traits; Autosomal Recessive Traits; X-Linked Recessive Traits; THE USE OF PEDIGREES TO PREDICT THE RESULTS OF MATINGS; Probability of Individual Genotypes; Probability of Group Outcomes; GATHERING DATA TO TEST THE MODE OF INHERITANCE OF A TRAIT
Pooling Data from Many Families and Ascertainment ErrorsAscertainment errors in studies of dominant traits; Ascertainment errors in studies of recessive traits; INHERITANCE OF MULTIPLE TRAITS: INDEPENDENT ASSORTMENT AND LINKAGE; Determination of Linkage from Human Pedigrees; Genetic Recombination and LOD Scores; Informative and Noninformative Matings; Neutral Polymorphisms, Marker Loci, and Genetic Maps; Box 1.2 Internet sites; The use of protein products to define marker loci; The use of directly detected DNA differences as marker lod EXAMPLE 1.1 Linkage of the Huntington's disease gene to an RFLPCONCLUSION; EXERCISES; REFERENCES; CHAPTER 2 Hereditary Traits That Do Not Show a Simple Mendelian Pattern; SINGLE-GENE TRAITS LACKING A SIMPLE MENDEUAN PATTERN; Variable Exprrssiviy and Incomplete Penetrance; Complementation; Phenocopies and Pleiotropy; QUANTITATIVE TRAITS; Multiple Alleles; Polygenic Inheritance; Major and Minor Genes; COMPLEX TRAITS; Epidemiological Analysis of Complex Traits; Liability; Family Clustering; Identical Twins; LOCALIZATION OF GENES RESPONSIBLE FOR COMPLEX AND QUANTITATIVE TRAITS Linkage Analysis of Complex TraitsAffected Pedigree Member (APM) or Allele-Sharing Methods; Example 2.1. Familial psoriasis; Example 2.2. Familial breast cancer; Analysis of quantitative trait loci by allele-sharing methods; Example 2.3. Insulin-dependent diabetes mellitus; Example 2.4. Male homosexuality; Allelic Association; Example 2.5. Dyslexia; Candidate Gene; Example 2.6. Nonsyndromal autosomal recessive deafness; Example 2.7. Neuroticism and genes for serotonin metabolism; CONCLUSION: NATURE VERSUS NURTURE; EXERCISES; REFERENCES; CHAPTER 3 Genome Organization I UNEXPRESSED DNA, REPETITIVE AND UNIQUE SEQUENCESClustered, Highly Repetitive Sequences; The main families of highly repetitive sequences; Example 3.1. The a family of highly repetitive DNA; Small-Cluster, Intermediately Repeated DNA; Minisatellite DNA; Microsatellite DNA; Dispersed, Intermediately Repeated Sequences; Viral retrotransposons; Nonviral retrotransposons: Alu, L1, and processed pseudogenes; Unique Sequence DNA; EXPRESSED DNA, GENES AND GENE FAMILIES; The Organization of RNA Polymerase I1 Genes: Intmns and Exons; Box 3.1. Internet sites; Example 3.2. Collagen Example 3.3. Cystic fibrosis |
Record Nr. | UNINA-9910145420503321 |
Maroni Gustavo
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||
Malden, MA, : Blackwell Science, c2001 | ||
![]() | ||
Lo trovi qui: Univ. Federico II | ||
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Molecular and genetic analysis of human traits [[electronic resource] /] / Gustavo Maroni |
Autore | Maroni Gustavo |
Pubbl/distr/stampa | Malden, MA, : Blackwell Science, c2001 |
Descrizione fisica | 1 online resource (296 p.) |
Disciplina | 599.935 |
Soggetto topico |
Human genetics
Medical genetics |
ISBN |
1-281-32161-3
9786611321611 0-470-76007-9 0-470-75980-1 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Contents; PREFACE; CHAPTER 1 The Inheritance of Simple Mendelian Traits in Humans; DETECTING MENDELIAN INHERITANCE IN HUMANS; Test-Crosses and Pure Lines versus Pedigrees and Inferred Genotypes; Box 1.1 Early observations of Mendelian inheritance in humans; PATTERNS OF INHERITANCE AND EXAMPLES; Autosomal Dominant Traits; Autosomal Recessive Traits; X-Linked Recessive Traits; THE USE OF PEDIGREES TO PREDICT THE RESULTS OF MATINGS; Probability of Individual Genotypes; Probability of Group Outcomes; GATHERING DATA TO TEST THE MODE OF INHERITANCE OF A TRAIT
Pooling Data from Many Families and Ascertainment ErrorsAscertainment errors in studies of dominant traits; Ascertainment errors in studies of recessive traits; INHERITANCE OF MULTIPLE TRAITS: INDEPENDENT ASSORTMENT AND LINKAGE; Determination of Linkage from Human Pedigrees; Genetic Recombination and LOD Scores; Informative and Noninformative Matings; Neutral Polymorphisms, Marker Loci, and Genetic Maps; Box 1.2 Internet sites; The use of protein products to define marker loci; The use of directly detected DNA differences as marker lod EXAMPLE 1.1 Linkage of the Huntington's disease gene to an RFLPCONCLUSION; EXERCISES; REFERENCES; CHAPTER 2 Hereditary Traits That Do Not Show a Simple Mendelian Pattern; SINGLE-GENE TRAITS LACKING A SIMPLE MENDEUAN PATTERN; Variable Exprrssiviy and Incomplete Penetrance; Complementation; Phenocopies and Pleiotropy; QUANTITATIVE TRAITS; Multiple Alleles; Polygenic Inheritance; Major and Minor Genes; COMPLEX TRAITS; Epidemiological Analysis of Complex Traits; Liability; Family Clustering; Identical Twins; LOCALIZATION OF GENES RESPONSIBLE FOR COMPLEX AND QUANTITATIVE TRAITS Linkage Analysis of Complex TraitsAffected Pedigree Member (APM) or Allele-Sharing Methods; Example 2.1. Familial psoriasis; Example 2.2. Familial breast cancer; Analysis of quantitative trait loci by allele-sharing methods; Example 2.3. Insulin-dependent diabetes mellitus; Example 2.4. Male homosexuality; Allelic Association; Example 2.5. Dyslexia; Candidate Gene; Example 2.6. Nonsyndromal autosomal recessive deafness; Example 2.7. Neuroticism and genes for serotonin metabolism; CONCLUSION: NATURE VERSUS NURTURE; EXERCISES; REFERENCES; CHAPTER 3 Genome Organization I UNEXPRESSED DNA, REPETITIVE AND UNIQUE SEQUENCESClustered, Highly Repetitive Sequences; The main families of highly repetitive sequences; Example 3.1. The a family of highly repetitive DNA; Small-Cluster, Intermediately Repeated DNA; Minisatellite DNA; Microsatellite DNA; Dispersed, Intermediately Repeated Sequences; Viral retrotransposons; Nonviral retrotransposons: Alu, L1, and processed pseudogenes; Unique Sequence DNA; EXPRESSED DNA, GENES AND GENE FAMILIES; The Organization of RNA Polymerase I1 Genes: Intmns and Exons; Box 3.1. Internet sites; Example 3.2. Collagen Example 3.3. Cystic fibrosis |
Record Nr. | UNISA-996218292203316 |
Maroni Gustavo
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||
Malden, MA, : Blackwell Science, c2001 | ||
![]() | ||
Lo trovi qui: Univ. di Salerno | ||
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Molecular and genetic analysis of human traits [[electronic resource] /] / Gustavo Maroni |
Autore | Maroni Gustavo |
Pubbl/distr/stampa | Malden, MA, : Blackwell Science, c2001 |
Descrizione fisica | 1 online resource (296 p.) |
Disciplina | 599.935 |
Soggetto topico |
Human genetics
Medical genetics |
ISBN |
1-281-32161-3
9786611321611 0-470-76007-9 0-470-75980-1 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Contents; PREFACE; CHAPTER 1 The Inheritance of Simple Mendelian Traits in Humans; DETECTING MENDELIAN INHERITANCE IN HUMANS; Test-Crosses and Pure Lines versus Pedigrees and Inferred Genotypes; Box 1.1 Early observations of Mendelian inheritance in humans; PATTERNS OF INHERITANCE AND EXAMPLES; Autosomal Dominant Traits; Autosomal Recessive Traits; X-Linked Recessive Traits; THE USE OF PEDIGREES TO PREDICT THE RESULTS OF MATINGS; Probability of Individual Genotypes; Probability of Group Outcomes; GATHERING DATA TO TEST THE MODE OF INHERITANCE OF A TRAIT
Pooling Data from Many Families and Ascertainment ErrorsAscertainment errors in studies of dominant traits; Ascertainment errors in studies of recessive traits; INHERITANCE OF MULTIPLE TRAITS: INDEPENDENT ASSORTMENT AND LINKAGE; Determination of Linkage from Human Pedigrees; Genetic Recombination and LOD Scores; Informative and Noninformative Matings; Neutral Polymorphisms, Marker Loci, and Genetic Maps; Box 1.2 Internet sites; The use of protein products to define marker loci; The use of directly detected DNA differences as marker lod EXAMPLE 1.1 Linkage of the Huntington's disease gene to an RFLPCONCLUSION; EXERCISES; REFERENCES; CHAPTER 2 Hereditary Traits That Do Not Show a Simple Mendelian Pattern; SINGLE-GENE TRAITS LACKING A SIMPLE MENDEUAN PATTERN; Variable Exprrssiviy and Incomplete Penetrance; Complementation; Phenocopies and Pleiotropy; QUANTITATIVE TRAITS; Multiple Alleles; Polygenic Inheritance; Major and Minor Genes; COMPLEX TRAITS; Epidemiological Analysis of Complex Traits; Liability; Family Clustering; Identical Twins; LOCALIZATION OF GENES RESPONSIBLE FOR COMPLEX AND QUANTITATIVE TRAITS Linkage Analysis of Complex TraitsAffected Pedigree Member (APM) or Allele-Sharing Methods; Example 2.1. Familial psoriasis; Example 2.2. Familial breast cancer; Analysis of quantitative trait loci by allele-sharing methods; Example 2.3. Insulin-dependent diabetes mellitus; Example 2.4. Male homosexuality; Allelic Association; Example 2.5. Dyslexia; Candidate Gene; Example 2.6. Nonsyndromal autosomal recessive deafness; Example 2.7. Neuroticism and genes for serotonin metabolism; CONCLUSION: NATURE VERSUS NURTURE; EXERCISES; REFERENCES; CHAPTER 3 Genome Organization I UNEXPRESSED DNA, REPETITIVE AND UNIQUE SEQUENCESClustered, Highly Repetitive Sequences; The main families of highly repetitive sequences; Example 3.1. The a family of highly repetitive DNA; Small-Cluster, Intermediately Repeated DNA; Minisatellite DNA; Microsatellite DNA; Dispersed, Intermediately Repeated Sequences; Viral retrotransposons; Nonviral retrotransposons: Alu, L1, and processed pseudogenes; Unique Sequence DNA; EXPRESSED DNA, GENES AND GENE FAMILIES; The Organization of RNA Polymerase I1 Genes: Intmns and Exons; Box 3.1. Internet sites; Example 3.2. Collagen Example 3.3. Cystic fibrosis |
Record Nr. | UNINA-9910830937203321 |
Maroni Gustavo
![]() |
||
Malden, MA, : Blackwell Science, c2001 | ||
![]() | ||
Lo trovi qui: Univ. Federico II | ||
|
Molecular and genetic analysis of human traits [[electronic resource] /] / Gustavo Maroni |
Autore | Maroni Gustavo |
Pubbl/distr/stampa | Malden, MA, : Blackwell Science, c2001 |
Descrizione fisica | 1 online resource (296 p.) |
Disciplina | 599.935 |
Soggetto topico |
Human genetics
Medical genetics |
ISBN |
1-281-32161-3
9786611321611 0-470-76007-9 0-470-75980-1 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Contents; PREFACE; CHAPTER 1 The Inheritance of Simple Mendelian Traits in Humans; DETECTING MENDELIAN INHERITANCE IN HUMANS; Test-Crosses and Pure Lines versus Pedigrees and Inferred Genotypes; Box 1.1 Early observations of Mendelian inheritance in humans; PATTERNS OF INHERITANCE AND EXAMPLES; Autosomal Dominant Traits; Autosomal Recessive Traits; X-Linked Recessive Traits; THE USE OF PEDIGREES TO PREDICT THE RESULTS OF MATINGS; Probability of Individual Genotypes; Probability of Group Outcomes; GATHERING DATA TO TEST THE MODE OF INHERITANCE OF A TRAIT
Pooling Data from Many Families and Ascertainment ErrorsAscertainment errors in studies of dominant traits; Ascertainment errors in studies of recessive traits; INHERITANCE OF MULTIPLE TRAITS: INDEPENDENT ASSORTMENT AND LINKAGE; Determination of Linkage from Human Pedigrees; Genetic Recombination and LOD Scores; Informative and Noninformative Matings; Neutral Polymorphisms, Marker Loci, and Genetic Maps; Box 1.2 Internet sites; The use of protein products to define marker loci; The use of directly detected DNA differences as marker lod EXAMPLE 1.1 Linkage of the Huntington's disease gene to an RFLPCONCLUSION; EXERCISES; REFERENCES; CHAPTER 2 Hereditary Traits That Do Not Show a Simple Mendelian Pattern; SINGLE-GENE TRAITS LACKING A SIMPLE MENDEUAN PATTERN; Variable Exprrssiviy and Incomplete Penetrance; Complementation; Phenocopies and Pleiotropy; QUANTITATIVE TRAITS; Multiple Alleles; Polygenic Inheritance; Major and Minor Genes; COMPLEX TRAITS; Epidemiological Analysis of Complex Traits; Liability; Family Clustering; Identical Twins; LOCALIZATION OF GENES RESPONSIBLE FOR COMPLEX AND QUANTITATIVE TRAITS Linkage Analysis of Complex TraitsAffected Pedigree Member (APM) or Allele-Sharing Methods; Example 2.1. Familial psoriasis; Example 2.2. Familial breast cancer; Analysis of quantitative trait loci by allele-sharing methods; Example 2.3. Insulin-dependent diabetes mellitus; Example 2.4. Male homosexuality; Allelic Association; Example 2.5. Dyslexia; Candidate Gene; Example 2.6. Nonsyndromal autosomal recessive deafness; Example 2.7. Neuroticism and genes for serotonin metabolism; CONCLUSION: NATURE VERSUS NURTURE; EXERCISES; REFERENCES; CHAPTER 3 Genome Organization I UNEXPRESSED DNA, REPETITIVE AND UNIQUE SEQUENCESClustered, Highly Repetitive Sequences; The main families of highly repetitive sequences; Example 3.1. The a family of highly repetitive DNA; Small-Cluster, Intermediately Repeated DNA; Minisatellite DNA; Microsatellite DNA; Dispersed, Intermediately Repeated Sequences; Viral retrotransposons; Nonviral retrotransposons: Alu, L1, and processed pseudogenes; Unique Sequence DNA; EXPRESSED DNA, GENES AND GENE FAMILIES; The Organization of RNA Polymerase I1 Genes: Intmns and Exons; Box 3.1. Internet sites; Example 3.2. Collagen Example 3.3. Cystic fibrosis |
Record Nr. | UNINA-9910841271503321 |
Maroni Gustavo
![]() |
||
Malden, MA, : Blackwell Science, c2001 | ||
![]() | ||
Lo trovi qui: Univ. Federico II | ||
|