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H Zierler

Showing results (21-30 of 24) with videos related to

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Journal of Medical Genetics|February 24, 2001
A de novo complex chromosomal rearrangement involving chromosomes 2, 3, and 10 associated with microcephaly and early onset spasticityW Emberger, E Petek, B Plecko-Starting, et al.
The British Journal of Ophthalmology|September 20, 2005
Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosaA Schuster, N Weisschuh, H Jägle, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 23, 2000
Clinical, cytogenetic and molecular analysis of three 46,XX malesE Plöchl, I Vlasak, O Rittinger, et al.
American Journal of Human Genetics|January 13, 2000
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)E Holinski-Feder, E Reyniers, S Uhrig, et al.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Journal of Medical Genetics|February 24, 2001
A de novo complex chromosomal rearrangement involving chromosomes 2, 3, and 10 associated with microcephaly and early onset spasticityW Emberger, E Petek, B Plecko-Starting, et al.
The British Journal of Ophthalmology|September 20, 2005
Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosaA Schuster, N Weisschuh, H Jägle, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 23, 2000
Clinical, cytogenetic and molecular analysis of three 46,XX malesE Plöchl, I Vlasak, O Rittinger, et al.
American Journal of Human Genetics|January 13, 2000
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)E Holinski-Feder, E Reyniers, S Uhrig, et al.
Pageof 3