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L A Brueton

Showing results (1-10 of 23) with videos related to

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Journal of Medical Genetics|November 1, 1990
Craniodiaphyseal dysplasiaL A Brueton, R M Winter
Journal of Medical Genetics|April 1, 1990
Ellis-van creveld syndrome, Jeune syndrome, and renal-hepatic-pancreatic dysplasia: separate entities or disease spectrum?L A Brueton, M J Dillon, R M Winter
European Journal of Medical Genetics|March 15, 2006
Sensorineural deafness, enamel abnormalities and nail abnormalities: a case report of Heimler syndrome in identical twin girlsK R Ong, S Visram, S McKaig, et al.
Clinical Dysmorphology|January 29, 2000
MURCS association with encephalocele: report of a second caseM Suri, L A Brueton, N Venkatraman, et al.
Journal of Medical Genetics|March 1, 1990
Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?L A Brueton, S M Huson, B Farren, et al.
American Journal of Medical Genetics|January 10, 1997
VACTERL with hydrocephalus in twins due to Fanconi anemia (FA): mutation in the FAC geneP M Cox, R A Gibson, N Morgan, et al.
Journal of Medical Genetics|November 1, 1989
Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic featuresL A Brueton, J C Barber, S M Huson, et al.
British Medical Journal (Clinical Research Ed.)|March 14, 1987
Eczema herpeticum: a potentially fatal diseaseI R Sanderson, L A Brueton, M O Savage, et al.
Journal of Medical Genetics|October 1, 1992
The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7pL A Brueton, L van Herwerden, K A Chotai, et al.
Clinical Genetics|September 27, 2000
Chronic myelomonocytic leukaemia in a child with constitutional partial trisomy 8 mosaicismA F Brady, C S Waters, M J Pocha, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|November 1, 1990
Craniodiaphyseal dysplasiaL A Brueton, R M Winter
Journal of Medical Genetics|April 1, 1990
Ellis-van creveld syndrome, Jeune syndrome, and renal-hepatic-pancreatic dysplasia: separate entities or disease spectrum?L A Brueton, M J Dillon, R M Winter
European Journal of Medical Genetics|March 15, 2006
Sensorineural deafness, enamel abnormalities and nail abnormalities: a case report of Heimler syndrome in identical twin girlsK R Ong, S Visram, S McKaig, et al.
Clinical Dysmorphology|January 29, 2000
MURCS association with encephalocele: report of a second caseM Suri, L A Brueton, N Venkatraman, et al.
Journal of Medical Genetics|March 1, 1990
Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?L A Brueton, S M Huson, B Farren, et al.
American Journal of Medical Genetics|January 10, 1997
VACTERL with hydrocephalus in twins due to Fanconi anemia (FA): mutation in the FAC geneP M Cox, R A Gibson, N Morgan, et al.
Journal of Medical Genetics|November 1, 1989
Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic featuresL A Brueton, J C Barber, S M Huson, et al.
British Medical Journal (Clinical Research Ed.)|March 14, 1987
Eczema herpeticum: a potentially fatal diseaseI R Sanderson, L A Brueton, M O Savage, et al.
Journal of Medical Genetics|October 1, 1992
The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7pL A Brueton, L van Herwerden, K A Chotai, et al.
Clinical Genetics|September 27, 2000
Chronic myelomonocytic leukaemia in a child with constitutional partial trisomy 8 mosaicismA F Brady, C S Waters, M J Pocha, et al.
Pageof 3