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Showing results (71-80 of 77) with videos related to

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American Journal of Human Genetics|October 27, 1997
A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)B Veldhuisen, J J Saris, S de Haij, et al.
American Journal of Human Genetics|October 23, 1997
Chorea-acanthocytosis: genetic linkage to chromosome 9q21J P Rubio, A Danek, C Stone, et al.
Nature Genetics|May 31, 2001
A conserved sorting-associated protein is mutant in chorea-acanthocytosisL Rampoldi, C Dobson-Stone, J P Rubio, et al.
Neurology|December 25, 2002
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathyE Nelis, S Erdem, P Y K Van Den Bergh, et al.
Cancer Genetics and Cytogenetics|June 19, 2007
Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?M Lessard, C Hélias, S Struski, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Molecular Syndromology|November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS SignL Desmyter, M Ghassibe, N Revencu, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
American Journal of Human Genetics|October 27, 1997
A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)B Veldhuisen, J J Saris, S de Haij, et al.
American Journal of Human Genetics|October 23, 1997
Chorea-acanthocytosis: genetic linkage to chromosome 9q21J P Rubio, A Danek, C Stone, et al.
Nature Genetics|May 31, 2001
A conserved sorting-associated protein is mutant in chorea-acanthocytosisL Rampoldi, C Dobson-Stone, J P Rubio, et al.
Neurology|December 25, 2002
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathyE Nelis, S Erdem, P Y K Van Den Bergh, et al.
Cancer Genetics and Cytogenetics|June 19, 2007
Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?M Lessard, C Hélias, S Struski, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Molecular Syndromology|November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS SignL Desmyter, M Ghassibe, N Revencu, et al.
Pageof 8