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J Schmidtke

Showing results (161-170 of 171) with videos related to

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Human Genetics|February 1, 1987
Regional localization and characterization of a DNA segment on the long arm of chromosome 21D N Cooper, S C Niemann, J R Gosden, et al.
Human Genetics|May 1, 1997
Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survivalM Macek, M Macek, A Krebsová, et al.
Clinical Genetics|May 9, 2008
Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23M Stuhrmann, H C Hennies, I A Bukhari, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.
Human Genetics|September 1, 1997
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferensT Dörk, B Dworniczak, C Aulehla-Scholz, et al.
QJM : Monthly Journal of the Association of Physicians|February 4, 2012
A simple clinical model to estimate the probability of Marfan syndromeS Sheikhzadeh, M L Kusch, M Rybczynski, et al.
Clinical Genetics|September 3, 2011
Analysis of phenotype and genotype information for the diagnosis of Marfan syndromeS Sheikhzadeh, C Kade, B Keyser, et al.
Human Genetics|June 1, 1996
Geographic distribution and origin of CFTR mutations in GermanyB Tümmler, T Storrs, V Dziadek, et al.
Molecular Syndromology|May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 MutationsM Alders, A Mendola, L Adès, et al.
American Journal of Human Genetics|June 19, 1998
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypesJ C Stephens, D E Reich, D B Goldstein, et al.
Pageof 18

Showing results (161-170 of 171) with videos related to

Sort By:
Pageof 18
Human Genetics|February 1, 1987
Regional localization and characterization of a DNA segment on the long arm of chromosome 21D N Cooper, S C Niemann, J R Gosden, et al.
Human Genetics|May 1, 1997
Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survivalM Macek, M Macek, A Krebsová, et al.
Clinical Genetics|May 9, 2008
Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23M Stuhrmann, H C Hennies, I A Bukhari, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.
Human Genetics|September 1, 1997
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferensT Dörk, B Dworniczak, C Aulehla-Scholz, et al.
QJM : Monthly Journal of the Association of Physicians|February 4, 2012
A simple clinical model to estimate the probability of Marfan syndromeS Sheikhzadeh, M L Kusch, M Rybczynski, et al.
Clinical Genetics|September 3, 2011
Analysis of phenotype and genotype information for the diagnosis of Marfan syndromeS Sheikhzadeh, C Kade, B Keyser, et al.
Human Genetics|June 1, 1996
Geographic distribution and origin of CFTR mutations in GermanyB Tümmler, T Storrs, V Dziadek, et al.
Molecular Syndromology|May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 MutationsM Alders, A Mendola, L Adès, et al.
American Journal of Human Genetics|June 19, 1998
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypesJ C Stephens, D E Reich, D B Goldstein, et al.
Pageof 18