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M Baraitser

Showing results (161-170 of 194) with videos related to

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Journal of Medical Genetics|September 1, 1987
Congenital cutis laxa with retardation of growth and developmentM A Patton, J Tolmie, P Ruthnum, et al.
Archives of Disease in Childhood|January 1, 1989
The 'happy puppet' syndrome of Angelman: review of the clinical featuresS A Robb, K R Pohl, M Baraitser, et al.
Journal of Medical Genetics|April 1, 1984
The 3-M syndromeR M Winter, M Baraitser, D B Grant, et al.
American Journal of Medical Genetics|September 15, 1991
Dominantly inherited syndrome comprising partially absent eye muscles, hydrocephaly, skeletal abnormalities, and a distinctive facial phenotypeL S Chitty, R McCrimmon, I K Temple, et al.
Journal of Medical Genetics|February 1, 1994
Partial trisomy 3q causing mild Cornelia de Lange phenotypeS E Holder, L M Grimsley, R W Palmer, et al.
American Journal of Medical Genetics|October 1, 1991
Genetic and clinical heterogeneity of Stickler syndromeG M Vintiner, I K Temple, H R Middleton-Price, et al.
Neuropediatrics|May 1, 1991
Pelizaeus-Merzbacher disease: classical or connatal?I E Scheffer, M Baraitser, J Wilson, et al.
The British Journal of Ophthalmology|October 1, 1991
Heterogeneity in dominant anterior segment malformationsG E Holmström, W P Reardon, M Baraitser, et al.
Clinical Genetics|June 1, 1985
The FG syndrome: 7 new casesE M Thompson, M Baraitser, R H Lindenbaum, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1984
Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological reportM Baraitser, W Gooddy, A M Halliday, et al.
Pageof 20

Showing results (161-170 of 194) with videos related to

Sort By:
Pageof 20
Journal of Medical Genetics|September 1, 1987
Congenital cutis laxa with retardation of growth and developmentM A Patton, J Tolmie, P Ruthnum, et al.
Archives of Disease in Childhood|January 1, 1989
The 'happy puppet' syndrome of Angelman: review of the clinical featuresS A Robb, K R Pohl, M Baraitser, et al.
Journal of Medical Genetics|April 1, 1984
The 3-M syndromeR M Winter, M Baraitser, D B Grant, et al.
American Journal of Medical Genetics|September 15, 1991
Dominantly inherited syndrome comprising partially absent eye muscles, hydrocephaly, skeletal abnormalities, and a distinctive facial phenotypeL S Chitty, R McCrimmon, I K Temple, et al.
Journal of Medical Genetics|February 1, 1994
Partial trisomy 3q causing mild Cornelia de Lange phenotypeS E Holder, L M Grimsley, R W Palmer, et al.
American Journal of Medical Genetics|October 1, 1991
Genetic and clinical heterogeneity of Stickler syndromeG M Vintiner, I K Temple, H R Middleton-Price, et al.
Neuropediatrics|May 1, 1991
Pelizaeus-Merzbacher disease: classical or connatal?I E Scheffer, M Baraitser, J Wilson, et al.
The British Journal of Ophthalmology|October 1, 1991
Heterogeneity in dominant anterior segment malformationsG E Holmström, W P Reardon, M Baraitser, et al.
Clinical Genetics|June 1, 1985
The FG syndrome: 7 new casesE M Thompson, M Baraitser, R H Lindenbaum, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1984
Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological reportM Baraitser, W Gooddy, A M Halliday, et al.
Pageof 20