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R M Winter

Showing results (161-170 of 219) with videos related to

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Clinical Dysmorphology|January 1, 1995
The natural history of human dermatosparaxis (Ehlers-Danlos syndrome type VIIC)W Reardon, R M Winter, L T Smith, et al.
American Journal of Medical Genetics|October 1, 1994
New autosomal dominant form of spondyloepiphyseal dysplasia presenting with atlanto-axial instabilityW Reardon, C M Hall, D G Shaw, et al.
Clinical Dysmorphology|May 29, 2000
The KBG syndromeS F Smithson, E M Thompson, A G McKinnon, et al.
Journal of Medical Genetics|September 3, 2002
Spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritanceC M Hall, N H Elcioglu, K D MacDermot, et al.
Lancet (London, England)|July 7, 1984
A clinically useful DNA probe closely linked to haemophilia AK Harper, R M Winter, M E Pembrey, et al.
Journal of Medical Genetics|March 1, 1995
Saethre-Chotzen syndrome associated with balanced translocations involving 7p21: three further familiesA O Wilkie, S P Yang, D Summers, et al.
Lancet (London, England)|December 1, 1984
X-chromosome-specific probe DX13 for carrier detection and first trimester prenatal diagnosis in haemophilia AT Tønnesen, F Søndergaard, M Mikkelsen, et al.
Journal of Medical Genetics|April 1, 1995
Alagille syndrome: family studiesF V Elmslie, A J Vivian, H Gardiner, et al.
Lancet (London, England)|January 5, 2002
PTEN mutations and proteus syndromeC Eng, H Thiele, X P Zhou, et al.
Clinical Dysmorphology|June 20, 2002
Hemifacial microsomia, external auditory canal atresia, deafness and Mullerian anomalies associated with acro-osteolysis: a new autosomal recessive syndrome?A F Brady, R M Winter, L C Wilson, et al.
Pageof 22

Showing results (161-170 of 219) with videos related to

Sort By:
Pageof 22
Clinical Dysmorphology|January 1, 1995
The natural history of human dermatosparaxis (Ehlers-Danlos syndrome type VIIC)W Reardon, R M Winter, L T Smith, et al.
American Journal of Medical Genetics|October 1, 1994
New autosomal dominant form of spondyloepiphyseal dysplasia presenting with atlanto-axial instabilityW Reardon, C M Hall, D G Shaw, et al.
Clinical Dysmorphology|May 29, 2000
The KBG syndromeS F Smithson, E M Thompson, A G McKinnon, et al.
Journal of Medical Genetics|September 3, 2002
Spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritanceC M Hall, N H Elcioglu, K D MacDermot, et al.
Lancet (London, England)|July 7, 1984
A clinically useful DNA probe closely linked to haemophilia AK Harper, R M Winter, M E Pembrey, et al.
Journal of Medical Genetics|March 1, 1995
Saethre-Chotzen syndrome associated with balanced translocations involving 7p21: three further familiesA O Wilkie, S P Yang, D Summers, et al.
Lancet (London, England)|December 1, 1984
X-chromosome-specific probe DX13 for carrier detection and first trimester prenatal diagnosis in haemophilia AT Tønnesen, F Søndergaard, M Mikkelsen, et al.
Journal of Medical Genetics|April 1, 1995
Alagille syndrome: family studiesF V Elmslie, A J Vivian, H Gardiner, et al.
Lancet (London, England)|January 5, 2002
PTEN mutations and proteus syndromeC Eng, H Thiele, X P Zhou, et al.
Clinical Dysmorphology|June 20, 2002
Hemifacial microsomia, external auditory canal atresia, deafness and Mullerian anomalies associated with acro-osteolysis: a new autosomal recessive syndrome?A F Brady, R M Winter, L C Wilson, et al.
Pageof 22