R M Winter|M E Pembrey - JoVE Visualize

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Clinical Dysmorphology|April 1, 1994

Mental retardation, microcephaly and blepharochalasis in brothersW Reardon, R M Winter, J Wilson, et al.

American Journal of Medical Genetics|December 11, 1996

Hemihypertrophy, hemimegalencephaly, and polydactylyW Reardon, B Harding, R M Winter, et al.

American Journal of Medical Genetics|January 1, 1988

Sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation: a possible "new" form of ectodermal dysplasiaR M Winter, K D MacDermot, F J Hill

Journal of Medical Genetics|June 1, 1986

A male infant with the Catel-Manzke syndrome and dislocatable kneesE M Thompson, R M Winter, M J Williams

Human Genetics|March 1, 1987

Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.

American Journal of Medical Genetics|May 1, 1988

Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysisA Hanauer, Y Alembik, S Gilgenkrantz, et al.

Lancet (London, England)|December 5, 1992

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNAW Reardon, R J Ross, M G Sweeney, et al.

Lancet (London, England)|March 23, 1991

Uniparental paternal disomy in Angelman's syndromeS Malcolm, J Clayton-Smith, M Nichols, et al.

Clinical Genetics|December 1, 1980

Osteopathia striata with cranial sclerosis: Highly variable expression within a family including cleft palate in two neonatal casesR M Winter, Crawfurd Md'A, H B Meire, et al.

American Journal of Medical Genetics|December 1, 1988

Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13L Brueton, S M Huson, R M Winter, et al.

Pageof 23

Showing results (101-110 of 230) with videos related to

Sort By:

Pageof 23

Clinical Dysmorphology|April 1, 1994

Mental retardation, microcephaly and blepharochalasis in brothersW Reardon, R M Winter, J Wilson, et al.

American Journal of Medical Genetics|December 11, 1996

Hemihypertrophy, hemimegalencephaly, and polydactylyW Reardon, B Harding, R M Winter, et al.

American Journal of Medical Genetics|January 1, 1988

Sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation: a possible "new" form of ectodermal dysplasiaR M Winter, K D MacDermot, F J Hill

Journal of Medical Genetics|June 1, 1986

A male infant with the Catel-Manzke syndrome and dislocatable kneesE M Thompson, R M Winter, M J Williams

Human Genetics|March 1, 1987

Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.

American Journal of Medical Genetics|May 1, 1988

Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysisA Hanauer, Y Alembik, S Gilgenkrantz, et al.

Lancet (London, England)|December 5, 1992

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNAW Reardon, R J Ross, M G Sweeney, et al.

Lancet (London, England)|March 23, 1991

Uniparental paternal disomy in Angelman's syndromeS Malcolm, J Clayton-Smith, M Nichols, et al.

Clinical Genetics|December 1, 1980

Osteopathia striata with cranial sclerosis: Highly variable expression within a family including cleft palate in two neonatal casesR M Winter, Crawfurd Md'A, H B Meire, et al.

American Journal of Medical Genetics|December 1, 1988

Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13L Brueton, S M Huson, R M Winter, et al.

Pageof 23