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M Baraitser

Showing results (91-100 of 194) with videos related to

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Clinical Genetics|August 1, 1982
Lenz microphthalmia--a case reportM Baraitser, R M Winter, D S Taylor
Acta Ophthalmologica Scandinavica. Supplement|January 1, 1996
The Walker-Warburg or a new syndrome?M Baraitser, J Dossetor, S Slaney, et al.
Journal of Medical Genetics|June 1, 1991
The Holt-Oram syndromeJ A Hurst, C M Hall, M Baraitser
Developmental Medicine and Child Neurology|October 1, 1991
Severe microcephaly associated with congenital varicella infectionI E Scheffer, M Baraitser, E M Brett
Clinical Dysmorphology|January 1, 1994
Femoral hypoplasia unusual facies syndrome with preaxial polydactylyM Baraitser, W Reardon, C Oley, et al.
American Journal of Ophthalmology|April 15, 1986
Congenital trichomegaly, pigmentary retinal degeneration, and short statureM A Patton, A E Harding, M Baraitser
American Journal of Medical Genetics|December 1, 1987
A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiencyJ A Hurst, M Baraitser, R M Winter
Journal of Medical Genetics|August 1, 1993
A new form of familial ataxia, deafness, and mental retardationW Reardon, J Wilson, N Cavanagh, et al.
Journal of Medical Genetics|June 1, 1993
Cerebellar ataxia and ectodermal dysplasia in brothersM Baraitser, W Reardon, A McShane, et al.
Journal of Medical Genetics|April 1, 1982
Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia)A E Harding, C M Hall, M Baraitser
Pageof 20

Showing results (91-100 of 194) with videos related to

Sort By:
Pageof 20
Clinical Genetics|August 1, 1982
Lenz microphthalmia--a case reportM Baraitser, R M Winter, D S Taylor
Acta Ophthalmologica Scandinavica. Supplement|January 1, 1996
The Walker-Warburg or a new syndrome?M Baraitser, J Dossetor, S Slaney, et al.
Journal of Medical Genetics|June 1, 1991
The Holt-Oram syndromeJ A Hurst, C M Hall, M Baraitser
Developmental Medicine and Child Neurology|October 1, 1991
Severe microcephaly associated with congenital varicella infectionI E Scheffer, M Baraitser, E M Brett
Clinical Dysmorphology|January 1, 1994
Femoral hypoplasia unusual facies syndrome with preaxial polydactylyM Baraitser, W Reardon, C Oley, et al.
American Journal of Ophthalmology|April 15, 1986
Congenital trichomegaly, pigmentary retinal degeneration, and short statureM A Patton, A E Harding, M Baraitser
American Journal of Medical Genetics|December 1, 1987
A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiencyJ A Hurst, M Baraitser, R M Winter
Journal of Medical Genetics|August 1, 1993
A new form of familial ataxia, deafness, and mental retardationW Reardon, J Wilson, N Cavanagh, et al.
Journal of Medical Genetics|June 1, 1993
Cerebellar ataxia and ectodermal dysplasia in brothersM Baraitser, W Reardon, A McShane, et al.
Journal of Medical Genetics|April 1, 1982
Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia)A E Harding, C M Hall, M Baraitser
Pageof 20