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R M Winter

Showing results (131-140 of 219) with videos related to

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Neuropediatrics|December 19, 2003
Characterization of brain malformations in the Baraitser-Winter syndrome and review of the literatureM Rossi, R Guerrini, W B Dobyns, et al.
Neuropediatrics|February 1, 1994
Disordered peripheral nerve conduction in DOOR(S) syndromeW Reardon, S Boyd, M C Pitt, et al.
Journal of Medical Genetics|December 19, 2001
Detection of a large TBX5 deletion in a family with Holt-Oram syndromeS M Akrami, R M Winter, J D Brook, et al.
Journal of Medical Genetics|April 1, 1996
The dysmorphic human-mouse homology database (DHMHD): an interactive World-Wide Web resource for gene mappingC D Evans, A G Searle, A A Schinzel, et al.
Clinical Dysmorphology|April 1, 1996
Serpentine fibula syndrome: expansion of the phenotype with three affected siblingsE M Rosser, N P Mann, C M Hall, et al.
Human Molecular Genetics|August 1, 1997
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic casesC S Rose, P Patel, W Reardon, 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 22

Showing results (131-140 of 219) with videos related to

Sort By:
Pageof 22
Neuropediatrics|December 19, 2003
Characterization of brain malformations in the Baraitser-Winter syndrome and review of the literatureM Rossi, R Guerrini, W B Dobyns, et al.
Neuropediatrics|February 1, 1994
Disordered peripheral nerve conduction in DOOR(S) syndromeW Reardon, S Boyd, M C Pitt, et al.
Journal of Medical Genetics|December 19, 2001
Detection of a large TBX5 deletion in a family with Holt-Oram syndromeS M Akrami, R M Winter, J D Brook, et al.
Journal of Medical Genetics|April 1, 1996
The dysmorphic human-mouse homology database (DHMHD): an interactive World-Wide Web resource for gene mappingC D Evans, A G Searle, A A Schinzel, et al.
Clinical Dysmorphology|April 1, 1996
Serpentine fibula syndrome: expansion of the phenotype with three affected siblingsE M Rosser, N P Mann, C M Hall, et al.
Human Molecular Genetics|August 1, 1997
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic casesC S Rose, P Patel, W Reardon, 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 22