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Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
October 9, 2012
[Pregnancy and Ehlers-Danlos vascular syndrome: patients' care and complications]
E Dubruc, S Dupuis-Girod, P Khau Van Kien, et al.
Journal of Medical Genetics
|
May 12, 2000
A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss
L Morlé, M Bozon, N Alloisio, et al.
Nature Genetics
|
April 1, 1994
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12
D Bonnet, A Pelet, L Legeai-Mallet, et al.
Journal De Genetique Humaine
|
August 1, 1987
[Systematic neonatal detection of Duchenne's muscular dystrophy. Results after 10 years' of experience in Lyons (France)]
H Plauchu, M P Cordier, H N Carrier, et al.
American Journal of Medical Genetics
|
April 6, 2000
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)
C L Shovlin, A E Guttmacher, E Buscarini, et al.
European Journal of Human Genetics : EJHG
|
April 10, 1999
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss
N Alloisio, L Morlé, M Bozon, et al.
Human Molecular Genetics
|
May 1, 1994
A gene for hereditary multiple exostoses maps to chromosome 19p
M Le Merrer, L Legeai-Mallet, P M Jeannin, et al.
American Journal of Human Genetics
|
October 18, 2000
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15
L Morlé, M Bozon, J C Zech, et al.
Surgery
|
December 1, 1994
Pheochromocytoma as the first manifestation of von Hippel-Lindau disease
S Richard, C Beigelman, J M Duclos, et al.
Prenatal Diagnosis
|
July 13, 2002
First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13)
T Martin-Denavit, J Attia-Sobol, J Theuil, et al.
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of 12
Search research articles
Search
Showing results (91-100 of 116) with videos related to
Sort By:
Page
of 12
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
October 9, 2012
[Pregnancy and Ehlers-Danlos vascular syndrome: patients' care and complications]
E Dubruc, S Dupuis-Girod, P Khau Van Kien, et al.
Journal of Medical Genetics
|
May 12, 2000
A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss
L Morlé, M Bozon, N Alloisio, et al.
Nature Genetics
|
April 1, 1994
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12
D Bonnet, A Pelet, L Legeai-Mallet, et al.
Journal De Genetique Humaine
|
August 1, 1987
[Systematic neonatal detection of Duchenne's muscular dystrophy. Results after 10 years' of experience in Lyons (France)]
H Plauchu, M P Cordier, H N Carrier, et al.
American Journal of Medical Genetics
|
April 6, 2000
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)
C L Shovlin, A E Guttmacher, E Buscarini, et al.
European Journal of Human Genetics : EJHG
|
April 10, 1999
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss
N Alloisio, L Morlé, M Bozon, et al.
Human Molecular Genetics
|
May 1, 1994
A gene for hereditary multiple exostoses maps to chromosome 19p
M Le Merrer, L Legeai-Mallet, P M Jeannin, et al.
American Journal of Human Genetics
|
October 18, 2000
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15
L Morlé, M Bozon, J C Zech, et al.
Surgery
|
December 1, 1994
Pheochromocytoma as the first manifestation of von Hippel-Lindau disease
S Richard, C Beigelman, J M Duclos, et al.
Prenatal Diagnosis
|
July 13, 2002
First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13)
T Martin-Denavit, J Attia-Sobol, J Theuil, et al.
Page
of 12