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M E Pembrey

Showing results (21-30 of 99) with videos related to

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Journal of Medical Genetics|June 1, 1992
Angelman syndromeJ Clayton-Smith, M E Pembrey
British Journal of Haematology|April 1, 1983
The estimation of fetal haemoglobin in healthy adults by radioimmunoassayP C Rutland, M E Pembrey, T Davies
Nature|October 31, 1991
Isodisomy in BWS chromosomesA O Wilkie, S Malcolm, M E Pembrey
Journal of Clinical Pathology|August 1, 1972
Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturationM E Pembrey, P McWade, D J Weatherall
American Journal of Medical Genetics|August 1, 1985
A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardationM E Pembrey, R M Winter, K E Davies
Journal of Medical Genetics|February 1, 1985
Trigonocephaly and the Opitz C syndromeC Sargent, J Burn, M Baraitser, et al.
Science (New York, N.Y.)|March 27, 1981
F-cell production in sickle cell anemia: regulation by genes linked to beta-hemoglobin locusG J Dover, S H Boyer, M E Pembrey
Lancet (London, England)|December 24, 1977
alpha 1-antitrypsin phenotypes in rheumatoid arthritis and ankylosing spondylitisP D Buisseret, M E Pembrey, M H Lessof
Lancet (London, England)|February 7, 1970
Normal child after maternal thalidomide ingestion in critical period of pregnancyM E Pembrey, C A Clarke, M M Frais
Journal of Medical Genetics|July 1, 1990
Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasiaJ Goodship, S Malcolm, A Clarke, et al.
Pageof 10

Showing results (21-30 of 99) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|June 1, 1992
Angelman syndromeJ Clayton-Smith, M E Pembrey
British Journal of Haematology|April 1, 1983
The estimation of fetal haemoglobin in healthy adults by radioimmunoassayP C Rutland, M E Pembrey, T Davies
Nature|October 31, 1991
Isodisomy in BWS chromosomesA O Wilkie, S Malcolm, M E Pembrey
Journal of Clinical Pathology|August 1, 1972
Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturationM E Pembrey, P McWade, D J Weatherall
American Journal of Medical Genetics|August 1, 1985
A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardationM E Pembrey, R M Winter, K E Davies
Journal of Medical Genetics|February 1, 1985
Trigonocephaly and the Opitz C syndromeC Sargent, J Burn, M Baraitser, et al.
Science (New York, N.Y.)|March 27, 1981
F-cell production in sickle cell anemia: regulation by genes linked to beta-hemoglobin locusG J Dover, S H Boyer, M E Pembrey
Lancet (London, England)|December 24, 1977
alpha 1-antitrypsin phenotypes in rheumatoid arthritis and ankylosing spondylitisP D Buisseret, M E Pembrey, M H Lessof
Lancet (London, England)|February 7, 1970
Normal child after maternal thalidomide ingestion in critical period of pregnancyM E Pembrey, C A Clarke, M M Frais
Journal of Medical Genetics|July 1, 1990
Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasiaJ Goodship, S Malcolm, A Clarke, et al.
Pageof 10