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H Plauchu

Showing results (61-70 of 116) with videos related to

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American Journal of Medical Genetics|November 1, 1990
Malformations and minor anomalies in children whose mothers had prenatal diagnosis: comparison between CVS and amniocentesisP Kaplan, J Normandin, G N Wilson, et al.
Clinical Genetics|October 12, 2001
Hypermobility type of Ehlers-Danlos syndrome: influence of pregnanciesF Golfier, S Peyrol, J Attia-Sobol, et al.
Human Genetics|January 1, 1982
Detection of carriers for Duchenne muscular dystrophy. Quality control of creatine kinase assayH Plauchu, C Junien, I Maire, et al.
The Journal of Urology|September 19, 2000
Renal arteriovenous malformation requiring surgery in Rendu-Osler-Weber disease (hereditary hemorrhagic telangiectasia)M Ziani, C Valignat, J G Lopez, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 1, 1988
Familial extrahepatic biliary atresiaA Lachaux, B Descos, H Plauchu, et al.
Clinical Genetics|September 13, 2001
Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?T Martin-Denavit, S Duthel, S Giraud, et al.
American Journal of Medical Genetics|February 15, 2001
Lissencephaly type III, stippled epiphyses and loose, thick skin: a new recessively inherited syndromeH Plauchu, F Encha-Razavi, M Hermier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 5, 2001
[Diagnostic trap and difficulties of genetic counseling in a family with neuromuscular disease carriers]G Lesca, E Ollagnon-Roman, J Lachanat, et al.
Human Molecular Genetics|December 1, 1994
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalH Chaïb, G Lina-Granade, P Guilford, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1996
[Spontaneous colonic perforations revealing Ehlers-Danlos syndrome type IV]C Henry, S Geiss, E Wodey, et al.
Pageof 12

Showing results (61-70 of 116) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics|November 1, 1990
Malformations and minor anomalies in children whose mothers had prenatal diagnosis: comparison between CVS and amniocentesisP Kaplan, J Normandin, G N Wilson, et al.
Clinical Genetics|October 12, 2001
Hypermobility type of Ehlers-Danlos syndrome: influence of pregnanciesF Golfier, S Peyrol, J Attia-Sobol, et al.
Human Genetics|January 1, 1982
Detection of carriers for Duchenne muscular dystrophy. Quality control of creatine kinase assayH Plauchu, C Junien, I Maire, et al.
The Journal of Urology|September 19, 2000
Renal arteriovenous malformation requiring surgery in Rendu-Osler-Weber disease (hereditary hemorrhagic telangiectasia)M Ziani, C Valignat, J G Lopez, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 1, 1988
Familial extrahepatic biliary atresiaA Lachaux, B Descos, H Plauchu, et al.
Clinical Genetics|September 13, 2001
Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?T Martin-Denavit, S Duthel, S Giraud, et al.
American Journal of Medical Genetics|February 15, 2001
Lissencephaly type III, stippled epiphyses and loose, thick skin: a new recessively inherited syndromeH Plauchu, F Encha-Razavi, M Hermier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 5, 2001
[Diagnostic trap and difficulties of genetic counseling in a family with neuromuscular disease carriers]G Lesca, E Ollagnon-Roman, J Lachanat, et al.
Human Molecular Genetics|December 1, 1994
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalH Chaïb, G Lina-Granade, P Guilford, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1996
[Spontaneous colonic perforations revealing Ehlers-Danlos syndrome type IV]C Henry, S Geiss, E Wodey, et al.
Pageof 12