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Journal of Medical Genetics|September 9, 2000
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairmentT P Hutchin, M J Parker, I D Young, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2E Roberts, A P Jackson, A C Carradice, et al.
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Showing results (41-50 of 42) with videos related to

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Pageof 5
You have reached the last page of results.This site can display upto 42 results.
Journal of Medical Genetics|September 9, 2000
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairmentT P Hutchin, M J Parker, I D Young, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2E Roberts, A P Jackson, A C Carradice, et al.
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