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J M Connor

Showing results (91-100 of 181) with videos related to

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Human Genetics|June 1, 1994
Assignment of the gene encoding the human thyrotropin-releasing hormone receptor to 8q23 by fluorescence in situ hybridizationN Morrison, S M Duthie, E Boyd, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Identification of chromosome 21 materials using the whole chromosome 21 specific libraryM N Isa, E Boyd, T L Turner, et al.
Journal of Medical Genetics|June 1, 1984
Inv dup (15) with mental retardation but few dysmorphic featuresD H Gilmore, E Boyd, J P McClure, et al.
Journal of Medical Genetics|June 4, 1998
Prediction of liability to orofacial clefting using genetic and craniofacial data from parentsP A Mossey, R Arngrimsson, J McColl, et al.
Human Genetics|October 1, 1989
Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31A Theriault, E Boyd, S B Harrap, et al.
Human Genetics|June 1, 1990
Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1N Morrison, S B Harrap, J L Arriza, et al.
American Journal of Medical Genetics|July 1, 1987
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected childJ L Tolmie, M McNay, J B Stephenson, et al.
Human Genetics|April 1, 1986
Assignment of the gene for dyskeratosis congenita to Xq28J M Connor, D Gatherer, F C Gray, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Tuberous sclerosis: analysis of linkage to red cell and plasma protein markersJ M Connor, J R Yates, L Mann, et al.
Prenatal Diagnosis|June 1, 1995
Analysis of maternal serum alpha-fetoprotein and free beta human chorionic gonadotrophin in the first trimester: implications for Down's syndrome screeningE Berry, D A Aitken, J A Crossley, et al.
Pageof 19

Showing results (91-100 of 181) with videos related to

Sort By:
Pageof 19
Human Genetics|June 1, 1994
Assignment of the gene encoding the human thyrotropin-releasing hormone receptor to 8q23 by fluorescence in situ hybridizationN Morrison, S M Duthie, E Boyd, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Identification of chromosome 21 materials using the whole chromosome 21 specific libraryM N Isa, E Boyd, T L Turner, et al.
Journal of Medical Genetics|June 1, 1984
Inv dup (15) with mental retardation but few dysmorphic featuresD H Gilmore, E Boyd, J P McClure, et al.
Journal of Medical Genetics|June 4, 1998
Prediction of liability to orofacial clefting using genetic and craniofacial data from parentsP A Mossey, R Arngrimsson, J McColl, et al.
Human Genetics|October 1, 1989
Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31A Theriault, E Boyd, S B Harrap, et al.
Human Genetics|June 1, 1990
Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1N Morrison, S B Harrap, J L Arriza, et al.
American Journal of Medical Genetics|July 1, 1987
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected childJ L Tolmie, M McNay, J B Stephenson, et al.
Human Genetics|April 1, 1986
Assignment of the gene for dyskeratosis congenita to Xq28J M Connor, D Gatherer, F C Gray, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Tuberous sclerosis: analysis of linkage to red cell and plasma protein markersJ M Connor, J R Yates, L Mann, et al.
Prenatal Diagnosis|June 1, 1995
Analysis of maternal serum alpha-fetoprotein and free beta human chorionic gonadotrophin in the first trimester: implications for Down's syndrome screeningE Berry, D A Aitken, J A Crossley, et al.
Pageof 19