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M Baraitser

Showing results (131-140 of 194) with videos related to

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Journal of Medical Genetics|February 1, 1991
Pitfalls in counselling: the craniosynostosesR Marini, K Temple, L Chitty, et al.
Clinical Dysmorphology|January 29, 2000
Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients: a new syndrome?A S Plomp, M Baraitser, S F Slaney, et al.
Clinical Dysmorphology|April 1, 1996
PEHO or PEHO-like syndrome?L S Chitty, S Robb, C Berry, et al.
Clinical Dysmorphology|July 1, 1997
The autosomal dominant syndrome with congenital stapes ankylosis, broad thumbs and hyperopiaY Hilhorst-Hofstee, P M Watkin, C M Hall, et al.
Clinical Genetics|December 1, 1981
Intrafamilial correlation in Friedreich's ataxiaR M Winter, A E Harding, M Baraitser, et al.
American Journal of Medical Genetics|September 1, 1990
Midline facial defects with ocular colobomataI K Temple, H Brunner, B Jones, et al.
Journal of Medical Genetics|June 1, 1986
Tel Hashomer camptodactyly syndrome: report of a case with myopathic featuresM A Patton, K D McDermot, B D Lake, et al.
European Journal of Pediatrics|December 1, 1992
Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumourR G Grundy, J Pritchard, M Baraitser, et al.
American Journal of Human Genetics|October 1, 1992
Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosisS Strautnieks, P Rutland, R M Winter, et al.
Journal of Medical Genetics|December 1, 1990
Two brothers with heart defects and limb shortening: case reports and reviewW Reardon, J Hurst, T I Farag, et al.
Pageof 20

Showing results (131-140 of 194) with videos related to

Sort By:
Pageof 20
Journal of Medical Genetics|February 1, 1991
Pitfalls in counselling: the craniosynostosesR Marini, K Temple, L Chitty, et al.
Clinical Dysmorphology|January 29, 2000
Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients: a new syndrome?A S Plomp, M Baraitser, S F Slaney, et al.
Clinical Dysmorphology|April 1, 1996
PEHO or PEHO-like syndrome?L S Chitty, S Robb, C Berry, et al.
Clinical Dysmorphology|July 1, 1997
The autosomal dominant syndrome with congenital stapes ankylosis, broad thumbs and hyperopiaY Hilhorst-Hofstee, P M Watkin, C M Hall, et al.
Clinical Genetics|December 1, 1981
Intrafamilial correlation in Friedreich's ataxiaR M Winter, A E Harding, M Baraitser, et al.
American Journal of Medical Genetics|September 1, 1990
Midline facial defects with ocular colobomataI K Temple, H Brunner, B Jones, et al.
Journal of Medical Genetics|June 1, 1986
Tel Hashomer camptodactyly syndrome: report of a case with myopathic featuresM A Patton, K D McDermot, B D Lake, et al.
European Journal of Pediatrics|December 1, 1992
Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumourR G Grundy, J Pritchard, M Baraitser, et al.
American Journal of Human Genetics|October 1, 1992
Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosisS Strautnieks, P Rutland, R M Winter, et al.
Journal of Medical Genetics|December 1, 1990
Two brothers with heart defects and limb shortening: case reports and reviewW Reardon, J Hurst, T I Farag, et al.
Pageof 20