Presentation is loading. Please wait.

Presentation is loading. Please wait.

Meiotic Segregation Analysis of RB1 Alleles in Retinoblastoma Pedigrees by Use of Single-Sperm Typing  Anne Girardet, Mary Sara McPeek, Esther P. Leeflang,

Published byElisabeth Tucker Modified over 5 years ago

Similar presentations

Presentation on theme: "Meiotic Segregation Analysis of RB1 Alleles in Retinoblastoma Pedigrees by Use of Single-Sperm Typing  Anne Girardet, Mary Sara McPeek, Esther P. Leeflang,"— Presentation transcript:

1 Meiotic Segregation Analysis of RB1 Alleles in Retinoblastoma Pedigrees by Use of Single-Sperm Typing  Anne Girardet, Mary Sara McPeek, Esther P. Leeflang, Francis Munier, Norman Arnheim, Mireille Claustres, Franck Pellestor  The American Journal of Human Genetics  Volume 66, Issue 1, Pages (January 2000) DOI: /302715 Copyright © 2000 The American Society of Human Genetics Terms and Conditions

2 Figure 1 Pedigrees of families with hereditary retinoblastoma. Arrows point to sperm donors. Blackened, half-blackened, and hatched symbols denote patients with bilateral retinoblastoma, unilateral retinoblastoma, and bilateral retinoma, respectively. An asterisk (*) appearing above a symbol indicates an individual whose DNA sample was available for genotyping study. The American Journal of Human Genetics  , DOI: ( /302715) Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Download ppt "Meiotic Segregation Analysis of RB1 Alleles in Retinoblastoma Pedigrees by Use of Single-Sperm Typing  Anne Girardet, Mary Sara McPeek, Esther P. Leeflang,"

Similar presentations

Nuclear and Mitochondrial DNA Analysis of a 2,000-Year-Old Necropolis in the Egyin Gol Valley of Mongolia Christine Keyser-Tracqui, Eric Crubézy, Bertrand.

Nuclear and Mitochondrial DNA Analysis of a 2,000-Year-Old Necropolis in the Egyin Gol Valley of Mongolia Christine Keyser-Tracqui, Eric Crubézy, Bertrand.
Previous Estimates of Mitochondrial DNA Mutation Level Variance Did Not Account for Sampling Error: Comparing the mtDNA Genetic Bottleneck in Mice and.

Previous Estimates of Mitochondrial DNA Mutation Level Variance Did Not Account for Sampling Error: Comparing the mtDNA Genetic Bottleneck in Mice and.
Functional Analysis of the Neurofibromatosis Type 2 Protein by Means of Disease- Causing Point Mutations Renee P. Stokowski, David R. Cox The American.

Functional Analysis of the Neurofibromatosis Type 2 Protein by Means of Disease- Causing Point Mutations Renee P. Stokowski, David R. Cox The American.
Gene Preference in Maple Syrup Urine Disease Mary M. Nellis, Dean J. Danner The American Journal of Human Genetics Volume 68, Issue 1, Pages 232-237 (January.

Gene Preference in Maple Syrup Urine Disease Mary M. Nellis, Dean J. Danner The American Journal of Human Genetics Volume 68, Issue 1, Pages (January.
Genomewide Comparison of DNA Sequences between Humans and Chimpanzees Ingo Ebersberger, Dirk Metzler, Carsten Schwarz, Svante Pääbo The American Journal.

Genomewide Comparison of DNA Sequences between Humans and Chimpanzees Ingo Ebersberger, Dirk Metzler, Carsten Schwarz, Svante Pääbo The American Journal.
The Trimmed-Haplotype Test for Linkage Disequilibrium

The Trimmed-Haplotype Test for Linkage Disequilibrium
Anna Middleton, J. Hewison, R.F. Mueller 

Anna Middleton, J. Hewison, R.F. Mueller 
Figure Pedigrees of the SCA42 families identified in this study

Figure Pedigrees of the SCA42 families identified in this study
Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and.

Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and.
Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q  Alex Desautels, Gustavo Turecki, Jacques Montplaisir, Adolfo.

Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q  Alex Desautels, Gustavo Turecki, Jacques Montplaisir, Adolfo.
Anna Middleton, J. Hewison, R.F. Mueller 

Anna Middleton, J. Hewison, R.F. Mueller 
Genetic Linkage of Paget Disease of the Bone to Chromosome 18q

Genetic Linkage of Paget Disease of the Bone to Chromosome 18q
Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28

Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28
Autosomal Recessive Nonsyndromic Neurosensory Deafness at DFNB1 Not Associated with the Compound-Heterozygous GJB2 (Connexin 26) Genotype M34T/167delT 

Autosomal Recessive Nonsyndromic Neurosensory Deafness at DFNB1 Not Associated with the Compound-Heterozygous GJB2 (Connexin 26) Genotype M34T/167delT 
The Importance of Genealogy in Determining Genetic Associations with Complex Traits  Dina L. Newman, Mark Abney, Mary Sara McPeek, Carole Ober, Nancy J.

The Importance of Genealogy in Determining Genetic Associations with Complex Traits  Dina L. Newman, Mark Abney, Mary Sara McPeek, Carole Ober, Nancy J.
The APC I1307K Allele and BRCA-Associated Ovarian Cancer Risk

The APC I1307K Allele and BRCA-Associated Ovarian Cancer Risk
Localization of a Gene (MCUL1) for Multiple Cutaneous Leiomyomata and Uterine Fibroids to Chromosome 1q42.3-q43  N.A. Alam, S. Bevan, M. Churchman, E.

Localization of a Gene (MCUL1) for Multiple Cutaneous Leiomyomata and Uterine Fibroids to Chromosome 1q42.3-q43  N.A. Alam, S. Bevan, M. Churchman, E.
High Prevalence of Pathogenic Mutations in Patients with Early-Onset Dementia Detected by Sequence Analyses of Four Different Genes  Ulrich Finckh, Tomas.

High Prevalence of Pathogenic Mutations in Patients with Early-Onset Dementia Detected by Sequence Analyses of Four Different Genes  Ulrich Finckh, Tomas.
I. Silveira, I. Alonso, L. Guimarães, P. Mendonça, C. Santos, P

I. Silveira, I. Alonso, L. Guimarães, P. Mendonça, C. Santos, P
Accounting for Linkage in Family-Based Tests of Association with Missing Parental Genotypes  Eden R. Martin, Meredyth P. Bass, Elizabeth R. Hauser, Norman.

Accounting for Linkage in Family-Based Tests of Association with Missing Parental Genotypes  Eden R. Martin, Meredyth P. Bass, Elizabeth R. Hauser, Norman.

Similar presentations

Ads by Google