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M Pembrey

Showing results (21-30 of 48) with videos related to

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 20, 2001
The association of aneuploidy and mild fetal pyelectasis in an unselected population: the results of a multicenter studyP M Chudleigh, L S Chitty, M Pembrey, et al.
Journal of Medical Genetics|June 1, 1989
Dominantly inherited cleft lip and palate in two familiesK Temple, M Calvert, D Plint, et al.
Lancet (London, England)|June 7, 1997
Mannose-binding lectin alleles in a prospectively recruited UK population. The ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and ChildhoodR Mead, D Jack, M Pembrey, et al.
Acta Oto-Laryngologica|November 1, 1993
Neuro-otological function in X-linked hearing loss: a multipedigree assessment and correlation with other clinical parametersW Reardon, S Bellman, P Phelps, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 26, 1999
The significance of choroid plexus cysts in an unselected population: results of a multicenter studyL S Chitty, P Chudleigh, E Wright, et al.
Neuroradiology|January 1, 1991
X-linked deafness, stapes gushers and a distinctive defect of the inner earP D Phelps, W Reardon, M Pembrey, et al.
Archives of Disease in Childhood|November 1, 1983
Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter geneJ Mossman, S Blunt, R Stephens, et al.
American Journal of Ophthalmology|June 15, 1989
Follow-up and diagnostic reappraisal of 75 patients with Leber's congenital amaurosisS R Lambert, A Kriss, D Taylor, et al.
American Journal of Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.
Acta Oto-Laryngologica|July 1, 1996
Dips on Békésy or audioscan fail to identify carriers of autosomal recessive non-syndromic hearing lossM Cohen, M Francis, L M Luxon, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 20, 2001
The association of aneuploidy and mild fetal pyelectasis in an unselected population: the results of a multicenter studyP M Chudleigh, L S Chitty, M Pembrey, et al.
Journal of Medical Genetics|June 1, 1989
Dominantly inherited cleft lip and palate in two familiesK Temple, M Calvert, D Plint, et al.
Lancet (London, England)|June 7, 1997
Mannose-binding lectin alleles in a prospectively recruited UK population. The ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and ChildhoodR Mead, D Jack, M Pembrey, et al.
Acta Oto-Laryngologica|November 1, 1993
Neuro-otological function in X-linked hearing loss: a multipedigree assessment and correlation with other clinical parametersW Reardon, S Bellman, P Phelps, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 26, 1999
The significance of choroid plexus cysts in an unselected population: results of a multicenter studyL S Chitty, P Chudleigh, E Wright, et al.
Neuroradiology|January 1, 1991
X-linked deafness, stapes gushers and a distinctive defect of the inner earP D Phelps, W Reardon, M Pembrey, et al.
Archives of Disease in Childhood|November 1, 1983
Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter geneJ Mossman, S Blunt, R Stephens, et al.
American Journal of Ophthalmology|June 15, 1989
Follow-up and diagnostic reappraisal of 75 patients with Leber's congenital amaurosisS R Lambert, A Kriss, D Taylor, et al.
American Journal of Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.
Acta Oto-Laryngologica|July 1, 1996
Dips on Békésy or audioscan fail to identify carriers of autosomal recessive non-syndromic hearing lossM Cohen, M Francis, L M Luxon, et al.
Pageof 5