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I Kennerknecht

Showing results (41-50 of 44) with videos related to

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Leukemia|October 17, 2003
A cryptic insertion (17;15) on both chromosomes 17 with lack of PML-RARA expression in a case of atypical acute promyelocytic leukemiaJ Tchinda, S Volpert, R Liersch, et al.
Human Genetics|November 1, 1993
Molecular analysis of mutations in the gene FMR-1 segregating in fragile X familiesP Steinbach, D Wöhrle, G Tariverdian, et al.
American Journal of Medical Genetics|October 23, 1995
Agonadism in two sisters with XY gonosomal constitution, mental retardation, short stature, severely retarded bone age, and multiple extragenital malformations: a new autosomal recessive syndromeI Kennerknecht, P von Saurma, R Brenner, et al.
American Journal of Human Genetics|June 1, 1997
Characterization of FMR1 promoter elements by in vivo-footprinting analysisS Schwemmle, E de Graaff, H Deissler, et al.
Pageof 5

Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Leukemia|October 17, 2003
A cryptic insertion (17;15) on both chromosomes 17 with lack of PML-RARA expression in a case of atypical acute promyelocytic leukemiaJ Tchinda, S Volpert, R Liersch, et al.
Human Genetics|November 1, 1993
Molecular analysis of mutations in the gene FMR-1 segregating in fragile X familiesP Steinbach, D Wöhrle, G Tariverdian, et al.
American Journal of Medical Genetics|October 23, 1995
Agonadism in two sisters with XY gonosomal constitution, mental retardation, short stature, severely retarded bone age, and multiple extragenital malformations: a new autosomal recessive syndromeI Kennerknecht, P von Saurma, R Brenner, et al.
American Journal of Human Genetics|June 1, 1997
Characterization of FMR1 promoter elements by in vivo-footprinting analysisS Schwemmle, E de Graaff, H Deissler, et al.
Pageof 5