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J M Stoler

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2001
Malformations reported in chorionic villus sampling exposed children: a review and analytic synthesis of the literatureJ M Stoler, C K McGuirk, E Lieberman, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Successful long-term treatment of hepatic carnitine palmitoyltransferase I deficiency and a novel mutationJ M Stoler, M A Sabry, C Hanley, et al.
American Journal of Medical Genetics|June 8, 2001
Separation of amniotic membranes after amniocentesis in an individual with the classic form of EDS and haploinsufficiency for COL5A1 expressionJ M Stoler, B Bromley, M A Castro, et al.
Cytogenetic and Genome Research|January 14, 2010
Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old femaleP J Hulick, K M Noonan, S Kulkarni, et al.
The Journal of Pediatrics|September 17, 1998
The prenatal detection of significant alcohol exposure with maternal blood markersJ M Stoler, K S Huntington, C M Peterson, et al.
Community Genetics|March 24, 2007
Knowledge of and attitudes about Alzheimer disease genetics: report of a pilot survey and two focus groupsT J Moscarillo, H Holt, M Perman, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2001
Malformations reported in chorionic villus sampling exposed children: a review and analytic synthesis of the literatureJ M Stoler, C K McGuirk, E Lieberman, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Successful long-term treatment of hepatic carnitine palmitoyltransferase I deficiency and a novel mutationJ M Stoler, M A Sabry, C Hanley, et al.
American Journal of Medical Genetics|June 8, 2001
Separation of amniotic membranes after amniocentesis in an individual with the classic form of EDS and haploinsufficiency for COL5A1 expressionJ M Stoler, B Bromley, M A Castro, et al.
Cytogenetic and Genome Research|January 14, 2010
Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old femaleP J Hulick, K M Noonan, S Kulkarni, et al.
The Journal of Pediatrics|September 17, 1998
The prenatal detection of significant alcohol exposure with maternal blood markersJ M Stoler, K S Huntington, C M Peterson, et al.
Community Genetics|March 24, 2007
Knowledge of and attitudes about Alzheimer disease genetics: report of a pilot survey and two focus groupsT J Moscarillo, H Holt, M Perman, et al.
Pageof 2