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M E Pembrey

Showing results (61-70 of 99) with videos related to

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British Journal of Haematology|July 1, 1980
Hb F synthesis in sickle cell anaemia: a comparison of Saudi Arab cases with those of African originW G Wood, M E Pembrey, G R Serjeant, et al.
Archives of Disease in Childhood|April 1, 1991
Nesidioblastosis: evidence for autosomal recessive inheritanceD A Woolf, J V Leonard, R C Trembath, et al.
Nature Genetics|February 14, 1998
Localisation of a gene implicated in a severe speech and language disorderS E Fisher, F Vargha-Khadem, K E Watkins, et al.
Journal of Medical Genetics|December 1, 1987
Multiple pterygium syndrome: evolution of the phenotypeE M Thompson, D Donnai, M Baraitser, et al.
Lancet (London, England)|October 10, 1970
Familial sideroblastic anaemia: problem of Xg and X chromosome inactivationD J Weatherall, M E Pembrey, E G Hall, et al.
Lancet (London, England)|July 7, 1984
A clinically useful DNA probe closely linked to haemophilia AK Harper, R M Winter, M E Pembrey, et al.
Human Genetics|January 1, 1984
Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndromeK E Davies, K Harper, D Bonthron, et al.
Human Molecular Genetics|December 1, 1996
Mapping of DFN2 to Xq22J Tyson, S Bellman, V Newton, et al.
The New England Journal of Medicine|December 11, 1980
A new genetic basis for hemoglobin-H diseaseL Pressley, D R Higgs, J B Clegg, et al.
Journal of Medical Genetics|December 1, 1985
Prenatal diagnosis of ornithine carbamoyl transferase deficiency using a gene specific probeM E Pembrey, J M Old, J V Leonard, et al.
Pageof 10

Showing results (61-70 of 99) with videos related to

Sort By:
Pageof 10
British Journal of Haematology|July 1, 1980
Hb F synthesis in sickle cell anaemia: a comparison of Saudi Arab cases with those of African originW G Wood, M E Pembrey, G R Serjeant, et al.
Archives of Disease in Childhood|April 1, 1991
Nesidioblastosis: evidence for autosomal recessive inheritanceD A Woolf, J V Leonard, R C Trembath, et al.
Nature Genetics|February 14, 1998
Localisation of a gene implicated in a severe speech and language disorderS E Fisher, F Vargha-Khadem, K E Watkins, et al.
Journal of Medical Genetics|December 1, 1987
Multiple pterygium syndrome: evolution of the phenotypeE M Thompson, D Donnai, M Baraitser, et al.
Lancet (London, England)|October 10, 1970
Familial sideroblastic anaemia: problem of Xg and X chromosome inactivationD J Weatherall, M E Pembrey, E G Hall, et al.
Lancet (London, England)|July 7, 1984
A clinically useful DNA probe closely linked to haemophilia AK Harper, R M Winter, M E Pembrey, et al.
Human Genetics|January 1, 1984
Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndromeK E Davies, K Harper, D Bonthron, et al.
Human Molecular Genetics|December 1, 1996
Mapping of DFN2 to Xq22J Tyson, S Bellman, V Newton, et al.
The New England Journal of Medicine|December 11, 1980
A new genetic basis for hemoglobin-H diseaseL Pressley, D R Higgs, J B Clegg, et al.
Journal of Medical Genetics|December 1, 1985
Prenatal diagnosis of ornithine carbamoyl transferase deficiency using a gene specific probeM E Pembrey, J M Old, J V Leonard, et al.
Pageof 10