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American Journal of Medical Genetics
|
February 1, 1991
Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers
I A Glass, L A Pirrit, E M White, et al.
Annals of Clinical Biochemistry
|
September 1, 1994
First trimester biochemical screening for trisomy 21: the role of free beta hCG, alpha fetoprotein and pregnancy associated plasma protein A
K Spencer, D A Aitken, J A Crossley, et al.
Lancet (London, England)
|
March 21, 1987
Evidence that the gene for tuberous sclerosis is on chromosome 9
A E Fryer, A Chalmers, J M Connor, et al.
American Journal of Medical Genetics
|
October 1, 1985
Lethal neonatal chondrodysplasias in the West of Scotland 1970-1983 with a description of a thanatophoric, dysplasialike, autosomal recessive disorder, Glasgow variant
J M Connor, R A Connor, E M Sweet, et al.
Hypertension (Dallas, Tex. : 1979)
|
April 1, 1993
The angiotensin I converting enzyme gene and predisposition to high blood pressure
S B Harrap, H R Davidson, J M Connor, et al.
Journal of Medical Genetics
|
November 1, 1994
Possible role of imprinting in the Turner phenotype
C E Chu, M D Donaldson, C J Kelnar, et al.
American Journal of Medical Genetics
|
April 1, 1989
Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry
A Cooke, J L Tolmie, F J Glencross, et al.
Calcified Tissue International
|
August 12, 1999
Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressiva
A S Virdi, E M Shore, R O Oreffo, et al.
American Journal of Medical Genetics
|
August 1, 1992
Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experience
I A Glass, R G Del Mastro, W G Lanyon, et al.
Hypertension (Dallas, Tex. : 1979)
|
July 23, 1998
Human alpha-adducin gene, blood pressure, and sodium metabolism
A Kamitani, Z Y Wong, R Fraser, et al.
Page
of 19
Search research articles
Search
Showing results (151-160 of 181) with videos related to
Sort By:
Page
of 19
American Journal of Medical Genetics
|
February 1, 1991
Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers
I A Glass, L A Pirrit, E M White, et al.
Annals of Clinical Biochemistry
|
September 1, 1994
First trimester biochemical screening for trisomy 21: the role of free beta hCG, alpha fetoprotein and pregnancy associated plasma protein A
K Spencer, D A Aitken, J A Crossley, et al.
Lancet (London, England)
|
March 21, 1987
Evidence that the gene for tuberous sclerosis is on chromosome 9
A E Fryer, A Chalmers, J M Connor, et al.
American Journal of Medical Genetics
|
October 1, 1985
Lethal neonatal chondrodysplasias in the West of Scotland 1970-1983 with a description of a thanatophoric, dysplasialike, autosomal recessive disorder, Glasgow variant
J M Connor, R A Connor, E M Sweet, et al.
Hypertension (Dallas, Tex. : 1979)
|
April 1, 1993
The angiotensin I converting enzyme gene and predisposition to high blood pressure
S B Harrap, H R Davidson, J M Connor, et al.
Journal of Medical Genetics
|
November 1, 1994
Possible role of imprinting in the Turner phenotype
C E Chu, M D Donaldson, C J Kelnar, et al.
American Journal of Medical Genetics
|
April 1, 1989
Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry
A Cooke, J L Tolmie, F J Glencross, et al.
Calcified Tissue International
|
August 12, 1999
Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressiva
A S Virdi, E M Shore, R O Oreffo, et al.
American Journal of Medical Genetics
|
August 1, 1992
Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experience
I A Glass, R G Del Mastro, W G Lanyon, et al.
Hypertension (Dallas, Tex. : 1979)
|
July 23, 1998
Human alpha-adducin gene, blood pressure, and sodium metabolism
A Kamitani, Z Y Wong, R Fraser, et al.
Page
of 19