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Dan Geiger

Showing results (21-30 of 40) with videos related to

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BMC Medical Genomics|October 20, 2010
Admixture mapping of end stage kidney disease genetic susceptibility using estimated mutual information ancestry informative markersLiran I Shlush, Sivan Bercovici, Walter G Wasser, et al.
American Journal of Human Genetics|August 4, 2009
Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 genePaul Renbaum, Efrat Kellerman, Ranit Jaron, et al.
European Journal of Human Genetics : EJHG|February 11, 2010
Mammary-digital-nail (MDN) syndrome: a novel phenotype maps to human chromosome 22q12.3-13.1Mira Genzer-Nir, Morad Khayat, Leonid Kogan, et al.
Journal of Medical Genetics|March 22, 2019
Genetic linkage analysis of a large family identifies <i>FIGN</i> as a candidate modulator of reduced penetrance in heritable pulmonary arterial hypertensionPau Puigdevall, Lucilla Piccari, Isabel Blanco, et al.
Human Molecular Genetics|February 20, 2014
Induced pluripotent stem cells as a model for telomeric abnormalities in ICF type I syndromeShira Sagie, Erika Ellran, Hagar Katzir, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13Ginat Narkis, Daniella Landau, Esther Manor, et al.
Nature Genetics|June 6, 2006
Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger proteinRamon Y Birnbaum, Alex Zvulunov, Dafna Hallel-Halevy, et al.
American Journal of Human Genetics|September 9, 2006
A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosisOrit Topaz, Margarita Indelman, Ilana Chefetz, et al.
Bioinformatics (Oxford, England)|November 20, 2012
A system for exact and approximate genetic linkage analysis of SNP data in large pedigreesMark Silberstein, Omer Weissbrod, Lars Otten, et al.
Science (New York, N.Y.)|March 3, 2018
Quantitative analysis of population-scale family trees with millions of relativesJoanna Kaplanis, Assaf Gordon, Tal Shor, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
BMC Medical Genomics|October 20, 2010
Admixture mapping of end stage kidney disease genetic susceptibility using estimated mutual information ancestry informative markersLiran I Shlush, Sivan Bercovici, Walter G Wasser, et al.
American Journal of Human Genetics|August 4, 2009
Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 genePaul Renbaum, Efrat Kellerman, Ranit Jaron, et al.
European Journal of Human Genetics : EJHG|February 11, 2010
Mammary-digital-nail (MDN) syndrome: a novel phenotype maps to human chromosome 22q12.3-13.1Mira Genzer-Nir, Morad Khayat, Leonid Kogan, et al.
Journal of Medical Genetics|March 22, 2019
Genetic linkage analysis of a large family identifies <i>FIGN</i> as a candidate modulator of reduced penetrance in heritable pulmonary arterial hypertensionPau Puigdevall, Lucilla Piccari, Isabel Blanco, et al.
Human Molecular Genetics|February 20, 2014
Induced pluripotent stem cells as a model for telomeric abnormalities in ICF type I syndromeShira Sagie, Erika Ellran, Hagar Katzir, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13Ginat Narkis, Daniella Landau, Esther Manor, et al.
Nature Genetics|June 6, 2006
Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger proteinRamon Y Birnbaum, Alex Zvulunov, Dafna Hallel-Halevy, et al.
American Journal of Human Genetics|September 9, 2006
A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosisOrit Topaz, Margarita Indelman, Ilana Chefetz, et al.
Bioinformatics (Oxford, England)|November 20, 2012
A system for exact and approximate genetic linkage analysis of SNP data in large pedigreesMark Silberstein, Omer Weissbrod, Lars Otten, et al.
Science (New York, N.Y.)|March 3, 2018
Quantitative analysis of population-scale family trees with millions of relativesJoanna Kaplanis, Assaf Gordon, Tal Shor, et al.
Pageof 4