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M Baraitser

Showing results (171-180 of 194) with videos related to

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Neuropediatrics|August 1, 1989
Autosomal recessive microcephaly, mental retardation with nonpigmentary retinopathy and a distinctive electroretinogramM G Harbord, S R Lambert, A Kriss, et al.
Journal of Medical Genetics|December 1, 1987
Multiple pterygium syndrome: evolution of the phenotypeE M Thompson, D Donnai, M Baraitser, et al.
Clinical Dysmorphology|April 1, 1994
A case with blepharophimosis resembling Ohdo syndromeJ A Maat-Kievit, P J Milla, J E Collins, et al.
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.
Journal of Medical Genetics|February 1, 1997
Normal erythrocyte membrane Gs alpha bioactivity in two unrelated patients with acrodysostosisL C Wilson, M E Oude Luttikhuis, M Baraitser, et al.
Clinical Dysmorphology|April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiaeM Baraitser, F Stewart, R M Winter, et al.
Lancet (London, England)|November 3, 1990
Unusual presentation of fragile X syndromeI K Temple, M Baraitser, M E Pembrey, et al.
Journal of Medical Genetics|March 1, 1989
Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studiesM A Patton, F Giannelli, A J Francis, et al.
Journal of Medical Genetics|September 1, 1989
Moebius' syndrome with unilateral cerebellar hypoplasiaM G Harbord, J P Finn, M A Hall-Craggs, et al.
Neuropediatrics|August 1, 1989
Early onset leukodystrophy with distinct facial features in 2 siblingsM G Harbord, J P Finn, M A Hall-Craggs, et al.
Pageof 20

Showing results (171-180 of 194) with videos related to

Sort By:
Pageof 20
Neuropediatrics|August 1, 1989
Autosomal recessive microcephaly, mental retardation with nonpigmentary retinopathy and a distinctive electroretinogramM G Harbord, S R Lambert, A Kriss, et al.
Journal of Medical Genetics|December 1, 1987
Multiple pterygium syndrome: evolution of the phenotypeE M Thompson, D Donnai, M Baraitser, et al.
Clinical Dysmorphology|April 1, 1994
A case with blepharophimosis resembling Ohdo syndromeJ A Maat-Kievit, P J Milla, J E Collins, et al.
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.
Journal of Medical Genetics|February 1, 1997
Normal erythrocyte membrane Gs alpha bioactivity in two unrelated patients with acrodysostosisL C Wilson, M E Oude Luttikhuis, M Baraitser, et al.
Clinical Dysmorphology|April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiaeM Baraitser, F Stewart, R M Winter, et al.
Lancet (London, England)|November 3, 1990
Unusual presentation of fragile X syndromeI K Temple, M Baraitser, M E Pembrey, et al.
Journal of Medical Genetics|March 1, 1989
Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studiesM A Patton, F Giannelli, A J Francis, et al.
Journal of Medical Genetics|September 1, 1989
Moebius' syndrome with unilateral cerebellar hypoplasiaM G Harbord, J P Finn, M A Hall-Craggs, et al.
Neuropediatrics|August 1, 1989
Early onset leukodystrophy with distinct facial features in 2 siblingsM G Harbord, J P Finn, M A Hall-Craggs, et al.
Pageof 20