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M E Pembrey

Showing results (51-60 of 99) with videos related to

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Lancet (London, England)|April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiencyJ Goodship, S Malcolm, Y L Lau, et al.
Archives of Disease in Childhood|April 1, 1982
HLA typing as a method of genetic counselling in congenital adrenal hyperplasiaM O Savage, H Field, E Wolf, et al.
British Medical Journal|July 21, 1973
Thalassaemia in the BritishH H Knox-Macaulay, D J Weatherall, J B Clegg, et al.
Journal of Medical Genetics|June 1, 1993
Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndromeJ Clayton-Smith, T Webb, X J Cheng, et al.
British Journal of Haematology|February 1, 1975
Haemoglobin Bart's in Saudi ArabiaM E Pembrey, D J Weatherall, J B Clegg, et al.
Diabetologia|October 24, 2000
The Gly972Arg variant in insulin receptor substrate-1 is not associated with birth weight in contemporary English children. The ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and ChildhoodS Mason, K K Ong, M E Pembrey, et al.
Journal of Medical Genetics|July 1, 1989
Kyphomelic dysplasiaI K Temple, E M Thompson, C M Hall, et al.
Journal of Medical Genetics|May 1, 1993
Linkage analysis of infantile pyloric stenosis and markers from chromosome 9q11-q33: no evidence for a major gene in this candidate regionE Chung, R Coffey, K Parker, et al.
Lancet (London, England)|August 7, 1982
Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiencyC H Rodeck, A D Patrick, M E Pembrey, et al.
Lancet (London, England)|November 3, 1990
Unusual presentation of fragile X syndromeI K Temple, M Baraitser, M E Pembrey, et al.
Pageof 10

Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
Lancet (London, England)|April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiencyJ Goodship, S Malcolm, Y L Lau, et al.
Archives of Disease in Childhood|April 1, 1982
HLA typing as a method of genetic counselling in congenital adrenal hyperplasiaM O Savage, H Field, E Wolf, et al.
British Medical Journal|July 21, 1973
Thalassaemia in the BritishH H Knox-Macaulay, D J Weatherall, J B Clegg, et al.
Journal of Medical Genetics|June 1, 1993
Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndromeJ Clayton-Smith, T Webb, X J Cheng, et al.
British Journal of Haematology|February 1, 1975
Haemoglobin Bart's in Saudi ArabiaM E Pembrey, D J Weatherall, J B Clegg, et al.
Diabetologia|October 24, 2000
The Gly972Arg variant in insulin receptor substrate-1 is not associated with birth weight in contemporary English children. The ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and ChildhoodS Mason, K K Ong, M E Pembrey, et al.
Journal of Medical Genetics|July 1, 1989
Kyphomelic dysplasiaI K Temple, E M Thompson, C M Hall, et al.
Journal of Medical Genetics|May 1, 1993
Linkage analysis of infantile pyloric stenosis and markers from chromosome 9q11-q33: no evidence for a major gene in this candidate regionE Chung, R Coffey, K Parker, et al.
Lancet (London, England)|August 7, 1982
Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiencyC H Rodeck, A D Patrick, M E Pembrey, et al.
Lancet (London, England)|November 3, 1990
Unusual presentation of fragile X syndromeI K Temple, M Baraitser, M E Pembrey, et al.
Pageof 10