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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 immunodeficiency
J 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 hyperplasia
M O Savage, H Field, E Wolf, et al.
British Medical Journal
|
July 21, 1973
Thalassaemia in the British
H 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 syndrome
J Clayton-Smith, T Webb, X J Cheng, et al.
British Journal of Haematology
|
February 1, 1975
Haemoglobin Bart's in Saudi Arabia
M 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 Childhood
S Mason, K K Ong, M E Pembrey, et al.
Journal of Medical Genetics
|
July 1, 1989
Kyphomelic dysplasia
I 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 region
E Chung, R Coffey, K Parker, et al.
Lancet (London, England)
|
August 7, 1982
Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiency
C H Rodeck, A D Patrick, M E Pembrey, et al.
Lancet (London, England)
|
November 3, 1990
Unusual presentation of fragile X syndrome
I K Temple, M Baraitser, M E Pembrey, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 99) with videos related to
Sort By:
Page
of 10
Lancet (London, England)
|
April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiency
J 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 hyperplasia
M O Savage, H Field, E Wolf, et al.
British Medical Journal
|
July 21, 1973
Thalassaemia in the British
H 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 syndrome
J Clayton-Smith, T Webb, X J Cheng, et al.
British Journal of Haematology
|
February 1, 1975
Haemoglobin Bart's in Saudi Arabia
M 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 Childhood
S Mason, K K Ong, M E Pembrey, et al.
Journal of Medical Genetics
|
July 1, 1989
Kyphomelic dysplasia
I 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 region
E Chung, R Coffey, K Parker, et al.
Lancet (London, England)
|
August 7, 1982
Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiency
C H Rodeck, A D Patrick, M E Pembrey, et al.
Lancet (London, England)
|
November 3, 1990
Unusual presentation of fragile X syndrome
I K Temple, M Baraitser, M E Pembrey, et al.
Page
of 10