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R M Winter

Showing results (111-120 of 219) with videos related to

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Human Genetics|May 8, 2000
Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairsN J Prescott, M M Lees, R M Winter, et al.
Journal of Medical Genetics|March 1, 1990
Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?L A Brueton, S M Huson, B Farren, et al.
Clinical Genetics|March 22, 2001
Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLINC Bacchelli, F R Goodman, P J Scambler, et al.
Human Genetics|January 1, 1983
A maximum likelihood estimate of the sex ratio of mutation rates in haemophilia AR M Winter, E G Tuddenham, E Goldman, et al.
Journal of Medical Genetics|April 1, 1987
A previously undescribed syndrome of thoracic dysplasia and communicating hydrocephalus in two sibs, one diagnosed prenatally by ultrasoundR M Winter, S Campbell, J S Wigglesworth, et al.
Clinical Genetics|December 1, 1981
Intrafamilial correlation in Friedreich's ataxiaR M Winter, A E Harding, M Baraitser, et al.
Journal of Medical Genetics|January 5, 2002
Sponastrime dysplasia: presentation in infancyA C Offiah, M Lees, R M Winter, et al.
Journal of Medical Genetics|February 25, 1998
Familial persistent pulmonary hypertension of the newborn resulting from misalignment of the pulmonary vessels (congenital alveolar capillary dysplasia)H B Vassal, M Malone, A J Petros, et al.
American Journal of Human Genetics|October 1, 1992
Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosisS Strautnieks, P Rutland, R M Winter, et al.
Clinical Dysmorphology|May 8, 1998
Rapadilino syndrome--a non-Finnish caseS G Kant, M Baraitser, P J Milla, et al.
Pageof 22

Showing results (111-120 of 219) with videos related to

Sort By:
Pageof 22
Human Genetics|May 8, 2000
Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairsN J Prescott, M M Lees, R M Winter, et al.
Journal of Medical Genetics|March 1, 1990
Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?L A Brueton, S M Huson, B Farren, et al.
Clinical Genetics|March 22, 2001
Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLINC Bacchelli, F R Goodman, P J Scambler, et al.
Human Genetics|January 1, 1983
A maximum likelihood estimate of the sex ratio of mutation rates in haemophilia AR M Winter, E G Tuddenham, E Goldman, et al.
Journal of Medical Genetics|April 1, 1987
A previously undescribed syndrome of thoracic dysplasia and communicating hydrocephalus in two sibs, one diagnosed prenatally by ultrasoundR M Winter, S Campbell, J S Wigglesworth, et al.
Clinical Genetics|December 1, 1981
Intrafamilial correlation in Friedreich's ataxiaR M Winter, A E Harding, M Baraitser, et al.
Journal of Medical Genetics|January 5, 2002
Sponastrime dysplasia: presentation in infancyA C Offiah, M Lees, R M Winter, et al.
Journal of Medical Genetics|February 25, 1998
Familial persistent pulmonary hypertension of the newborn resulting from misalignment of the pulmonary vessels (congenital alveolar capillary dysplasia)H B Vassal, M Malone, A J Petros, et al.
American Journal of Human Genetics|October 1, 1992
Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosisS Strautnieks, P Rutland, R M Winter, et al.
Clinical Dysmorphology|May 8, 1998
Rapadilino syndrome--a non-Finnish caseS G Kant, M Baraitser, P J Milla, et al.
Pageof 22