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Journal of Medical Genetics
|
October 1, 1984
The femoral hypoplasia-unusual facies syndrome
J 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 patients
W 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 case
W Reardon, I K Temple, H Mackinnon, et al.
Neuropediatrics
|
February 1, 1992
Autosomal recessive microcephaly with severe psychomotor retardation
I 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 tale
J 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 patients
M A Patton, S Krywawych, R M Winter, et al.
Clinical Dysmorphology
|
April 1, 1994
Megalocornea, developmental retardation and dysmorphic features: two further patients
M 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 identity
R 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.
Page
of 20
Search research articles
Search
Showing results (151-160 of 194) with videos related to
Sort By:
Page
of 20
Journal of Medical Genetics
|
October 1, 1984
The femoral hypoplasia-unusual facies syndrome
J 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 patients
W 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 case
W Reardon, I K Temple, H Mackinnon, et al.
Neuropediatrics
|
February 1, 1992
Autosomal recessive microcephaly with severe psychomotor retardation
I 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 tale
J 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 patients
M A Patton, S Krywawych, R M Winter, et al.
Clinical Dysmorphology
|
April 1, 1994
Megalocornea, developmental retardation and dysmorphic features: two further patients
M 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 identity
R 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.
Page
of 20