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J A Crolla

Showing results (61-70 of 78) with videos related to

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Journal of Medical Genetics|March 1, 1997
A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locusJ A Crolla, J E Cawdery, C A Oley, et al.
American Journal of Medical Genetics. Part A|March 22, 2005
Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twinsDominique Brémond-Gignac, Marion Gérard-Blanluet, Henri Copin, et al.
American Journal of Medical Genetics|August 1, 1993
Mosaic tetrasomy 8p: molecular cytogenetic confirmation and measurement of glutathione reductase and tissue plasminogen activator levelsA M Fisher, J C Barber, J A Crolla, et al.
Human Genetics|January 1, 1997
Refined molecular characterization of the breakpoints in small inv dup(15) chromosomesB Huang, J A Crolla, S L Christian, et al.
Annals of Human Genetics|July 1, 1990
A cytogenetic and molecular reappraisal of a series of patients with Turner's syndromeP A Jacobs, P R Betts, A E Cockwell, et al.
Neurology|April 7, 2010
Pseudodominant inheritance of spastic ataxia of Charlevoix-SaguenayA Terracciano, N C Foulds, A Ditchfield, et al.
Journal of Medical Genetics|March 1, 1995
Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndromeJ N Macpherson, G Curtis, J A Crolla, et al.
Prenatal Diagnosis|July 1, 1996
Rapid in situ harvesting and cytogenetic analysis of perinatal tissue samplesA M Fisher, A E Cockwell, K J Moore, et al.
The Journal of Pediatrics|July 1, 1996
Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective studyS A Webber, E Hatchwell, J C Barber, et al.
Nature Genetics|February 1, 1995
An imprinted gene(s) for diabetes?I K Temple, R S James, J A Crolla, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|March 1, 1997
A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locusJ A Crolla, J E Cawdery, C A Oley, et al.
American Journal of Medical Genetics. Part A|March 22, 2005
Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twinsDominique Brémond-Gignac, Marion Gérard-Blanluet, Henri Copin, et al.
American Journal of Medical Genetics|August 1, 1993
Mosaic tetrasomy 8p: molecular cytogenetic confirmation and measurement of glutathione reductase and tissue plasminogen activator levelsA M Fisher, J C Barber, J A Crolla, et al.
Human Genetics|January 1, 1997
Refined molecular characterization of the breakpoints in small inv dup(15) chromosomesB Huang, J A Crolla, S L Christian, et al.
Annals of Human Genetics|July 1, 1990
A cytogenetic and molecular reappraisal of a series of patients with Turner's syndromeP A Jacobs, P R Betts, A E Cockwell, et al.
Neurology|April 7, 2010
Pseudodominant inheritance of spastic ataxia of Charlevoix-SaguenayA Terracciano, N C Foulds, A Ditchfield, et al.
Journal of Medical Genetics|March 1, 1995
Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndromeJ N Macpherson, G Curtis, J A Crolla, et al.
Prenatal Diagnosis|July 1, 1996
Rapid in situ harvesting and cytogenetic analysis of perinatal tissue samplesA M Fisher, A E Cockwell, K J Moore, et al.
The Journal of Pediatrics|July 1, 1996
Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective studyS A Webber, E Hatchwell, J C Barber, et al.
Nature Genetics|February 1, 1995
An imprinted gene(s) for diabetes?I K Temple, R S James, J A Crolla, et al.
Pageof 8