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D H Cohn

Showing results (41-50 of 66) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 1, 1983
Cloning of the Vibrio harveyi luciferase genes: use of a synthetic oligonucleotide probeD H Cohn, R C Ogden, J N Abelson, et al.
Genomics|December 1, 1993
Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19M D Briggs, I M Rasmussen, J L Weber, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22D Krakow, K Reinker, B Powell, et al.
Clinical Genetics|July 16, 2004
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Clinical Genetics|July 18, 2002
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
American Journal of Medical Genetics|August 26, 1998
Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindredM Ahmad, M Faiyaz Ul Haque, W Ahmad, et al.
Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.
Prenatal Diagnosis|July 1, 1993
First-trimester prenatal diagnosis of osteogenesis imperfecta type II by DNA analysis and sonographyM S DiMaio, R Barth, K E Koprivnikar, et al.
Genomics|December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19J T Hecht, C A Francomano, M D Briggs, et al.
Nature Genetics|September 1, 1993
A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaM L Warman, M Abbott, S S Apte, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1983
Cloning of the Vibrio harveyi luciferase genes: use of a synthetic oligonucleotide probeD H Cohn, R C Ogden, J N Abelson, et al.
Genomics|December 1, 1993
Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19M D Briggs, I M Rasmussen, J L Weber, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22D Krakow, K Reinker, B Powell, et al.
Clinical Genetics|July 16, 2004
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Clinical Genetics|July 18, 2002
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
American Journal of Medical Genetics|August 26, 1998
Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindredM Ahmad, M Faiyaz Ul Haque, W Ahmad, et al.
Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.
Prenatal Diagnosis|July 1, 1993
First-trimester prenatal diagnosis of osteogenesis imperfecta type II by DNA analysis and sonographyM S DiMaio, R Barth, K E Koprivnikar, et al.
Genomics|December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19J T Hecht, C A Francomano, M D Briggs, et al.
Nature Genetics|September 1, 1993
A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaM L Warman, M Abbott, S S Apte, et al.
Pageof 7