D Donnai|A P Read - JoVE Visualize

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Genomics|October 1, 1990

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets familiesR V Thakker, K E Davies, A P Read, et al.

Archives of Disease in Childhood|May 1, 1986

Recurrent neural tube defects, risk factors and vitaminsJ Wild, A P Read, S Sheppard, et al.

The British Journal of Dermatology|December 21, 2004

Coinheritance of two rare genodermatoses (Papillon-Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic studyC Hewitt, C-L Wu, F N Hattab, et al.

Human Genetics|July 1, 1986

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysisA P Read, R V Thakker, K E Davies, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractF R Goodman, S Mundlos, Y Muragaki, et al.

Clinical Genetics|September 19, 2008

A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndromeR Day, B Beckett, D Donnai, et al.

Lancet (London, England)|December 5, 1987

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophyS M Forrest, T J Smith, G S Cross, et al.

Human Molecular Genetics|January 15, 1999

EYA4, a novel vertebrate gene related to Drosophila eyes absentG Borsani, A DeGrandi, A Ballabio, et al.

Human Mutation|January 1, 1997

Nine novel L1 CAM mutations in families with X-linked hydrocephalusJ R MacFarlane, J S Du, M E Pepys, et al.

American Journal of Human Genetics|February 1, 1995

Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37L C Wilson, K Leverton, M E Oude Luttikhuis, et al.

Pageof 19

Showing results (161-170 of 185) with videos related to

Sort By:

Pageof 19

Genomics|October 1, 1990

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets familiesR V Thakker, K E Davies, A P Read, et al.

Archives of Disease in Childhood|May 1, 1986

Recurrent neural tube defects, risk factors and vitaminsJ Wild, A P Read, S Sheppard, et al.

The British Journal of Dermatology|December 21, 2004

Coinheritance of two rare genodermatoses (Papillon-Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic studyC Hewitt, C-L Wu, F N Hattab, et al.

Human Genetics|July 1, 1986

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysisA P Read, R V Thakker, K E Davies, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractF R Goodman, S Mundlos, Y Muragaki, et al.

Clinical Genetics|September 19, 2008

A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndromeR Day, B Beckett, D Donnai, et al.

Lancet (London, England)|December 5, 1987

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophyS M Forrest, T J Smith, G S Cross, et al.

Human Molecular Genetics|January 15, 1999

EYA4, a novel vertebrate gene related to Drosophila eyes absentG Borsani, A DeGrandi, A Ballabio, et al.

Human Mutation|January 1, 1997

Nine novel L1 CAM mutations in families with X-linked hydrocephalusJ R MacFarlane, J S Du, M E Pepys, et al.

American Journal of Human Genetics|February 1, 1995

Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37L C Wilson, K Leverton, M E Oude Luttikhuis, et al.

Pageof 19