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Human Genetics|March 1, 1996

Angelman syndrome in an inbred familyJ Beuten, R C Hennekam, B Van Roy, et al.

Leukemia|May 1, 1988

Karyotypic evidence for the leukemic involvement of the erythroblasts in erythroleukemiaZ N Berneman, D R van Bockstaele, M Van den Bergh, et al.

Nature Genetics|June 1, 1993

The full mutation in the FMR-1 gene of male fragile X patients is absent in their spermE Reyniers, L Vits, K De Boulle, et al.

Journal of Medical Genetics|July 1, 1995

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13qG Van Camp, M N Van Thienen, I Handig, et al.

Nature Genetics|January 1, 1993

A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.

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Showing results (11-20 of 15) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 15 results.

Human Genetics|March 1, 1996

Angelman syndrome in an inbred familyJ Beuten, R C Hennekam, B Van Roy, et al.

Leukemia|May 1, 1988

Karyotypic evidence for the leukemic involvement of the erythroblasts in erythroleukemiaZ N Berneman, D R van Bockstaele, M Van den Bergh, et al.

Nature Genetics|June 1, 1993

The full mutation in the FMR-1 gene of male fragile X patients is absent in their spermE Reyniers, L Vits, K De Boulle, et al.

Journal of Medical Genetics|July 1, 1995

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13qG Van Camp, M N Van Thienen, I Handig, et al.

Nature Genetics|January 1, 1993

A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.

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