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H Plauchu

Showing results (51-60 of 116) with videos related to

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World Journal of Surgery|July 1, 1981
Rectocolic familial polyposis: a study of 32 casesD Bigay, H Plauchu, P Berard, et al.
Annals of Human Biology|May 1, 1992
An abnormal concentration of cases of Rendu-Osler disease in the Valserine valley of the French Jura: a genealogical and demographic studyA Bideau, G Brunet, E Heyer, et al.
Pediatrie|January 1, 1987
[Scriver type autosomal hypophosphatemic rachitis: a family case]L David, J L Pesso, P Cochat, et al.
Journal De Genetique Humaine|June 1, 1980
[Genetic aspects of Rendu-Osler disease in Haut-Jura: convergence of methodological approaches of historic demography and medical genetics]A Bideau, H Plauchu, A Jacquard, et al.
Rhinology|July 12, 2011
Psychosocial quality of life in hereditary haemorrhagic telangiectasia patientsM Loaëc, S Morinière, M Hitier, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1985
[Trichorhinophalangeal syndrome. Apropos of a case]C Marchand, M H Villedieu, H Plauchu, et al.
Human Molecular Genetics|May 1, 1995
A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12qP Vincent, H Plauchu, J Hazan, et al.
Pediatrie|September 1, 1985
[A familial case of Rothmund-Thomson syndrome. A case in favor of the uniqueness of the syndrome. Association with osteosarcoma]P Rebaud, L David, H Plauchu, et al.
Lancet (London, England)|March 25, 1989
Duchenne muscular dystrophy: neonatal screening and prenatal diagnosisH Plauchu, C Dorche, M P Cordier, et al.
Pediatrie|December 1, 1975
[Lipo-atrophic diabetes]D Floret, B Longin, H Plauchu, et al.
Pageof 12

Showing results (51-60 of 116) with videos related to

Sort By:
Pageof 12
World Journal of Surgery|July 1, 1981
Rectocolic familial polyposis: a study of 32 casesD Bigay, H Plauchu, P Berard, et al.
Annals of Human Biology|May 1, 1992
An abnormal concentration of cases of Rendu-Osler disease in the Valserine valley of the French Jura: a genealogical and demographic studyA Bideau, G Brunet, E Heyer, et al.
Pediatrie|January 1, 1987
[Scriver type autosomal hypophosphatemic rachitis: a family case]L David, J L Pesso, P Cochat, et al.
Journal De Genetique Humaine|June 1, 1980
[Genetic aspects of Rendu-Osler disease in Haut-Jura: convergence of methodological approaches of historic demography and medical genetics]A Bideau, H Plauchu, A Jacquard, et al.
Rhinology|July 12, 2011
Psychosocial quality of life in hereditary haemorrhagic telangiectasia patientsM Loaëc, S Morinière, M Hitier, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1985
[Trichorhinophalangeal syndrome. Apropos of a case]C Marchand, M H Villedieu, H Plauchu, et al.
Human Molecular Genetics|May 1, 1995
A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12qP Vincent, H Plauchu, J Hazan, et al.
Pediatrie|September 1, 1985
[A familial case of Rothmund-Thomson syndrome. A case in favor of the uniqueness of the syndrome. Association with osteosarcoma]P Rebaud, L David, H Plauchu, et al.
Lancet (London, England)|March 25, 1989
Duchenne muscular dystrophy: neonatal screening and prenatal diagnosisH Plauchu, C Dorche, M P Cordier, et al.
Pediatrie|December 1, 1975
[Lipo-atrophic diabetes]D Floret, B Longin, H Plauchu, et al.
Pageof 12