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M Baraitser

Showing results (121-130 of 194) with videos related to

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Clinical Genetics|September 1, 1980
Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further caseR M Winter, D M Swallow, M Baraitser, et al.
Journal of Mental Deficiency Research|December 1, 1980
Organic acidurias and amino acidurias in the aetiology of long-term mental handicapR W Watts, M Baraitser, R A Chalmers, et al.
The Journal of Pediatrics|January 1, 1986
A distinctive type of hypohidrotic ectodermal dysplasia featuring hypothyroidismM G Pike, M Baraitser, R Dinwiddie, et al.
Journal of the Neurological Sciences|October 1, 1976
Axonal velocities of motor units in the hand and foot muscles of the baboonR W Gilliatt, H C Hopf, P Rudge, et al.
Journal of Medical Genetics|March 1, 1990
Focal dermal hypoplasia (Goltz syndrome)I K Temple, P MacDowall, M Baraitser, et al.
Journal of Medical Genetics|February 1, 1990
A familial syndrome of microcephaly, sparse hair, mental retardation, and seizuresA van Haeringen, J A Hurst, R Savidge, et al.
Journal of Medical Genetics|January 1, 1991
Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'K D MacDermot, R M Winter, D Taylor, et al.
Acta Neurologica Scandinavica|November 11, 2009
Natural history, symptoms and treatment of the narcoleptic syndromeJ D Parkes, M Baraitser, C D Marsden, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1982
Joubert-Boltshauser syndrome with polydactyly in siblingsJ Egger, M H Bellman, E M Ross, et al.
American Journal of Medical Genetics|January 30, 1995
Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndromeW Reardon, R J Gibbons, R M Winter, et al.
Pageof 20

Showing results (121-130 of 194) with videos related to

Sort By:
Pageof 20
Clinical Genetics|September 1, 1980
Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further caseR M Winter, D M Swallow, M Baraitser, et al.
Journal of Mental Deficiency Research|December 1, 1980
Organic acidurias and amino acidurias in the aetiology of long-term mental handicapR W Watts, M Baraitser, R A Chalmers, et al.
The Journal of Pediatrics|January 1, 1986
A distinctive type of hypohidrotic ectodermal dysplasia featuring hypothyroidismM G Pike, M Baraitser, R Dinwiddie, et al.
Journal of the Neurological Sciences|October 1, 1976
Axonal velocities of motor units in the hand and foot muscles of the baboonR W Gilliatt, H C Hopf, P Rudge, et al.
Journal of Medical Genetics|March 1, 1990
Focal dermal hypoplasia (Goltz syndrome)I K Temple, P MacDowall, M Baraitser, et al.
Journal of Medical Genetics|February 1, 1990
A familial syndrome of microcephaly, sparse hair, mental retardation, and seizuresA van Haeringen, J A Hurst, R Savidge, et al.
Journal of Medical Genetics|January 1, 1991
Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'K D MacDermot, R M Winter, D Taylor, et al.
Acta Neurologica Scandinavica|November 11, 2009
Natural history, symptoms and treatment of the narcoleptic syndromeJ D Parkes, M Baraitser, C D Marsden, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1982
Joubert-Boltshauser syndrome with polydactyly in siblingsJ Egger, M H Bellman, E M Ross, et al.
American Journal of Medical Genetics|January 30, 1995
Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndromeW Reardon, R J Gibbons, R M Winter, et al.
Pageof 20