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M Baraitser

Showing results (151-160 of 194) with videos related to

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Journal of Medical Genetics|October 1, 1984
The femoral hypoplasia-unusual facies syndromeJ Burn, R M Winter, M Baraitser, et al.
Brain : a Journal of Neurology|June 1, 1980
The incidence and nature of visual pathway involvement in Friedreich's ataxia. A clinical and visual evoked potential study of 22 patientsW M Carroll, A Kriss, M Baraitser, et al.
Clinical Dysmorphology|July 1, 1996
Nance-Sweeney chondrodysplasia--a further case?E M Rosser, C M Hall, J Harper, et al.
Clinical Genetics|November 1, 1990
Partial lipodystrophy syndromes--a further male caseW Reardon, I K Temple, H Mackinnon, et al.
Neuropediatrics|February 1, 1992
Autosomal recessive microcephaly with severe psychomotor retardationI E Scheffer, M Baraitser, J Wilson, et al.
Pediatric Cardiology|January 1, 1984
Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: a cautionary taleJ Burn, M Baraitser, D T Hughes, et al.
American Journal of Medical Genetics|January 1, 1987
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patientsM A Patton, S Krywawych, R M Winter, et al.
Clinical Dysmorphology|April 1, 1994
Megalocornea, developmental retardation and dysmorphic features: two further patientsM L Gibbs, A O Wilkie, R M Winter, et al.
American Journal of Medical Genetics|October 1, 1983
The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identityR M Winter, M Baraitser, K M Laurence, et al.
Journal of Medical Genetics|May 1, 1989
Moore-Federman syndrome and acromicric dysplasia: are they the same entity?R M Winter, M A Patton, J Challener, et al.
Pageof 20

Showing results (151-160 of 194) with videos related to

Sort By:
Pageof 20
Journal of Medical Genetics|October 1, 1984
The femoral hypoplasia-unusual facies syndromeJ Burn, R M Winter, M Baraitser, et al.
Brain : a Journal of Neurology|June 1, 1980
The incidence and nature of visual pathway involvement in Friedreich's ataxia. A clinical and visual evoked potential study of 22 patientsW M Carroll, A Kriss, M Baraitser, et al.
Clinical Dysmorphology|July 1, 1996
Nance-Sweeney chondrodysplasia--a further case?E M Rosser, C M Hall, J Harper, et al.
Clinical Genetics|November 1, 1990
Partial lipodystrophy syndromes--a further male caseW Reardon, I K Temple, H Mackinnon, et al.
Neuropediatrics|February 1, 1992
Autosomal recessive microcephaly with severe psychomotor retardationI E Scheffer, M Baraitser, J Wilson, et al.
Pediatric Cardiology|January 1, 1984
Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: a cautionary taleJ Burn, M Baraitser, D T Hughes, et al.
American Journal of Medical Genetics|January 1, 1987
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patientsM A Patton, S Krywawych, R M Winter, et al.
Clinical Dysmorphology|April 1, 1994
Megalocornea, developmental retardation and dysmorphic features: two further patientsM L Gibbs, A O Wilkie, R M Winter, et al.
American Journal of Medical Genetics|October 1, 1983
The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identityR M Winter, M Baraitser, K M Laurence, et al.
Journal of Medical Genetics|May 1, 1989
Moore-Federman syndrome and acromicric dysplasia: are they the same entity?R M Winter, M A Patton, J Challener, et al.
Pageof 20