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J M Connor

Showing results (61-70 of 181) with videos related to

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Journal of Medical Genetics|July 1, 1993
Dyskeratosis congenita: three additional families show linkage to a locus in Xq28R Arngrimsson, I Dokal, L Luzzatto, et al.
Journal of Clinical Psychology|April 1, 1980
A comparison of three covert assertion training proceduresC T Twentyman, D R Pharr, J M Connor
Human Genetics|July 1, 1992
Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6pL Izquierdo, M Porteous, P G Paramo, et al.
Human Molecular Genetics|April 1, 1995
Characterisation of a novel splice donor mutation affecting position +1 in intron 18 of the NF-1 geneS M Purandare, W G Lanyon, R Arngrimsson, et al.
Prenatal Diagnosis|November 1, 1996
Insulin-dependent diabetes mellitus and prenatal screening results: current experience from a regional screening programmeJ A Crossley, E Berry, D A Aitken, et al.
Journal of Medical Screening|July 1, 1994
Impact of a regional screening programme using maternal serum alpha fetoprotein (AFP) and human chorionic gonadotrophin (hCG) on the birth incidence of Down's syndrome in the west of ScotlandJ A Crossley, D A Aitken, E Berry, et al.
Placenta|March 29, 2000
Placental synthesis of oestriol in Down's syndrome pregnanciesD Newby, D A Aitken, A G Howatson, et al.
Gut|August 1, 1986
Monozygous twins concordant for duodenojejunal villous atrophy and dermatitis herpetiformisS T Green, S Natarajan, J M Connor, et al.
Lancet (London, England)|June 13, 1992
Free beta-hCG as first-trimester marker for fetal trisomyK Spencer, J N Macri, D A Aitken, et al.
The Journal of Investigative Dermatology|August 12, 1998
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomasR M MacKie, N Andrew, W G Lanyon, et al.
Pageof 19

Showing results (61-70 of 181) with videos related to

Sort By:
Pageof 19
Journal of Medical Genetics|July 1, 1993
Dyskeratosis congenita: three additional families show linkage to a locus in Xq28R Arngrimsson, I Dokal, L Luzzatto, et al.
Journal of Clinical Psychology|April 1, 1980
A comparison of three covert assertion training proceduresC T Twentyman, D R Pharr, J M Connor
Human Genetics|July 1, 1992
Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6pL Izquierdo, M Porteous, P G Paramo, et al.
Human Molecular Genetics|April 1, 1995
Characterisation of a novel splice donor mutation affecting position +1 in intron 18 of the NF-1 geneS M Purandare, W G Lanyon, R Arngrimsson, et al.
Prenatal Diagnosis|November 1, 1996
Insulin-dependent diabetes mellitus and prenatal screening results: current experience from a regional screening programmeJ A Crossley, E Berry, D A Aitken, et al.
Journal of Medical Screening|July 1, 1994
Impact of a regional screening programme using maternal serum alpha fetoprotein (AFP) and human chorionic gonadotrophin (hCG) on the birth incidence of Down's syndrome in the west of ScotlandJ A Crossley, D A Aitken, E Berry, et al.
Placenta|March 29, 2000
Placental synthesis of oestriol in Down's syndrome pregnanciesD Newby, D A Aitken, A G Howatson, et al.
Gut|August 1, 1986
Monozygous twins concordant for duodenojejunal villous atrophy and dermatitis herpetiformisS T Green, S Natarajan, J M Connor, et al.
Lancet (London, England)|June 13, 1992
Free beta-hCG as first-trimester marker for fetal trisomyK Spencer, J N Macri, D A Aitken, et al.
The Journal of Investigative Dermatology|August 12, 1998
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomasR M MacKie, N Andrew, W G Lanyon, et al.
Pageof 19