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Human Genetics|February 1, 1996

Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletionS Debrus, G Berger, A de Meeus, et al.

Human Genetics|July 1, 1995

Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literatureS Demczuk, A Lévy, M Aubry, et al.

Human Genetics|January 28, 1999

Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African familyF Macari, C Lautier, A Girardet, et al.

Journal of Molecular and Cellular Cardiology|May 1, 1997

Lack of evidence for connexin 43 gene mutations in human autosomal recessive lateralization defectsS Debrus, S Tuffery, R Matsuoka, et al.

Clinical Genetics|August 23, 2006

Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndromeG Millat, P Chevalier, L Restier-Miron, et al.

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Showing results (41-50 of 45) with videos related to

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You have reached the last page of results.This site can display upto 45 results.

Human Genetics|February 1, 1996

Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletionS Debrus, G Berger, A de Meeus, et al.

Human Genetics|July 1, 1995

Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literatureS Demczuk, A Lévy, M Aubry, et al.

Human Genetics|January 28, 1999

Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African familyF Macari, C Lautier, A Girardet, et al.

Journal of Molecular and Cellular Cardiology|May 1, 1997

Lack of evidence for connexin 43 gene mutations in human autosomal recessive lateralization defectsS Debrus, S Tuffery, R Matsuoka, et al.

Clinical Genetics|August 23, 2006

Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndromeG Millat, P Chevalier, L Restier-Miron, et al.

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