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G Sekhon

Showing results (1-10 of 10) with videos related to

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Cancer|November 1, 1977
Chromosomal aberrations in human neuroblastomasG M Brodeur, G Sekhon, M N Goldstein
American Journal of Medical Genetics|June 27, 1997
Del(10)(q22.3q24.1) associated with juvenile polyposisR F Jacoby, S Schlack, G Sekhon, et al.
Archives of Pediatrics & Adolescent Medicine|May 30, 1998
Pathological case of the month. Chromosome 10 qter deletion syndromeD T Costakos, L A Love, K Josephson, et al.
Annals of Cardiac Anaesthesia|July 14, 2017
An antenatal diagnosis: Congenital high airway obstructionS Miital, A Mittal, R Singal, et al.
Genomics|April 1, 1991
Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qterR G Gregg, A B Metzenberg, K Hogan, et al.
Systematic Reviews|December 19, 2025
The impact of socioeconomic determinants of health and resulting health inequalities on children and young people with long-term health conditions in the UK: a scoping review protocolG Sekhon, J Wray, A Ifederu, et al.
Clinical Genetics|April 1, 1976
Partial trisomy 5 with a carrier parent t(5p-;9p+)P Monteleone, J Monteleone, G Sekhon, et al.
Somatic Cell and Molecular Genetics|November 1, 1986
Derepression of HPRT locus on inactive X chromosome of human lymphoblastoid cell lineN Nadon, G Sekhon, L J Brown, et al.
Human Genetics|March 10, 1999
Delineation of two distinct 6p deletion syndromesA F Davies, G Mirza, G Sekhon, et al.
American Journal of Medical Genetics|November 1, 1988
Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysisA O Martin, H Northrup, D H Ledbetter, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Cancer|November 1, 1977
Chromosomal aberrations in human neuroblastomasG M Brodeur, G Sekhon, M N Goldstein
American Journal of Medical Genetics|June 27, 1997
Del(10)(q22.3q24.1) associated with juvenile polyposisR F Jacoby, S Schlack, G Sekhon, et al.
Archives of Pediatrics & Adolescent Medicine|May 30, 1998
Pathological case of the month. Chromosome 10 qter deletion syndromeD T Costakos, L A Love, K Josephson, et al.
Annals of Cardiac Anaesthesia|July 14, 2017
An antenatal diagnosis: Congenital high airway obstructionS Miital, A Mittal, R Singal, et al.
Genomics|April 1, 1991
Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qterR G Gregg, A B Metzenberg, K Hogan, et al.
Systematic Reviews|December 19, 2025
The impact of socioeconomic determinants of health and resulting health inequalities on children and young people with long-term health conditions in the UK: a scoping review protocolG Sekhon, J Wray, A Ifederu, et al.
Clinical Genetics|April 1, 1976
Partial trisomy 5 with a carrier parent t(5p-;9p+)P Monteleone, J Monteleone, G Sekhon, et al.
Somatic Cell and Molecular Genetics|November 1, 1986
Derepression of HPRT locus on inactive X chromosome of human lymphoblastoid cell lineN Nadon, G Sekhon, L J Brown, et al.
Human Genetics|March 10, 1999
Delineation of two distinct 6p deletion syndromesA F Davies, G Mirza, G Sekhon, et al.
American Journal of Medical Genetics|November 1, 1988
Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysisA O Martin, H Northrup, D H Ledbetter, et al.
Pageof 1