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H Plauchu

Showing results (71-80 of 116) with videos related to

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Journal De Genetique Humaine|March 1, 1981
[Early clinical and histopathological manifestations in 14 boys showing elevated serum creatine-phosphokinase levels in their first year]P Guibaud, H N Carrier, H Plauchu, et al.
Gastroenterologie Clinique Et Biologique|February 19, 2000
[Hepatic vascular malformations in Rendu-Osler disease]J C Saurin, J Dumortier, Y Menard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 1, 1995
[Spontaneous colonic perforations revealing Ehlers-Danlos syndrome type IV]C Henry, S Geiss, E Wodey, et al.
Annales De Genetique|January 1, 1984
[Association of VACTERL and hydrocephalus: a new familial entity]M L Briard, M le Merrer, H Plauchu, et al.
La Revue De Medecine Interne|July 28, 1999
[Vascular Ehlers-Danlos syndrome. Diagnosis 17 years after first digestive manifestations]T Zenone, C Grange, P Pelissier, et al.
Journal De Genetique Humaine|March 1, 1981
[Neonatal screening for duchenne myopathy by serum elevation of creatine phosphokinase activity. 5 years experience]H Plauchu, C Dellamonica, B Pascal, et al.
Pediatrie|January 1, 1992
[Sacrum abnormalities and neural tube closure defect: different manifestations of a same genetic disease?]E Cavero Vargas, H Plauchu, A Rebaud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 29, 2001
[Genetic deafness:the primary cause of sensorineural hearing loss in children]G Lina-Granade, L Morlé, N Alloisio, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1981
[Gonadic dysgenesis and dicentric chromosome Y. A report of two cases, one of which had a gonadoblastoma (author's transl)]H Plauchu, G Magnin, C Laurent, et al.
American Journal of Medical Genetics|October 20, 2000
Ectodermal abnormalities associated with methimazole intrauterine exposureT Martin-Denavit, P Edery, H Plauchu, et al.
Pageof 12

Showing results (71-80 of 116) with videos related to

Sort By:
Pageof 12
Journal De Genetique Humaine|March 1, 1981
[Early clinical and histopathological manifestations in 14 boys showing elevated serum creatine-phosphokinase levels in their first year]P Guibaud, H N Carrier, H Plauchu, et al.
Gastroenterologie Clinique Et Biologique|February 19, 2000
[Hepatic vascular malformations in Rendu-Osler disease]J C Saurin, J Dumortier, Y Menard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 1, 1995
[Spontaneous colonic perforations revealing Ehlers-Danlos syndrome type IV]C Henry, S Geiss, E Wodey, et al.
Annales De Genetique|January 1, 1984
[Association of VACTERL and hydrocephalus: a new familial entity]M L Briard, M le Merrer, H Plauchu, et al.
La Revue De Medecine Interne|July 28, 1999
[Vascular Ehlers-Danlos syndrome. Diagnosis 17 years after first digestive manifestations]T Zenone, C Grange, P Pelissier, et al.
Journal De Genetique Humaine|March 1, 1981
[Neonatal screening for duchenne myopathy by serum elevation of creatine phosphokinase activity. 5 years experience]H Plauchu, C Dellamonica, B Pascal, et al.
Pediatrie|January 1, 1992
[Sacrum abnormalities and neural tube closure defect: different manifestations of a same genetic disease?]E Cavero Vargas, H Plauchu, A Rebaud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 29, 2001
[Genetic deafness:the primary cause of sensorineural hearing loss in children]G Lina-Granade, L Morlé, N Alloisio, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1981
[Gonadic dysgenesis and dicentric chromosome Y. A report of two cases, one of which had a gonadoblastoma (author's transl)]H Plauchu, G Magnin, C Laurent, et al.
American Journal of Medical Genetics|October 20, 2000
Ectodermal abnormalities associated with methimazole intrauterine exposureT Martin-Denavit, P Edery, H Plauchu, et al.
Pageof 12