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H Plauchu

Showing results (81-90 of 116) with videos related to

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Neurology|December 10, 2008
Stroke following pulmonary arteriovenous fistula embolization in a patient with HHTS Felix, S Jeannin, C Goizet, et al.
Radiology|January 1, 1985
Small, asymptomatic angiomyolipomas of the kidneyP M Bret, M Bretagnolle, D Gaillard, et al.
Nature|June 10, 1998
Connexin 26 gene linked to a dominant deafnessF Denoyelle, G Lina-Granade, H Plauchu, et al.
Gastroenterology|December 31, 1998
Liver transplantation resolves the hyperdynamic circulation in hereditary hemorrhagic telangiectasia with hepatic involvementO Boillot, F Bianco, J P Viale, et al.
Pediatrie|April 1, 1975
[Triploidy in the child. I. Study of phenotype. An observation of triploidy with mosaicism 46, XX/69, XXY]M David, A Chambon, C Laurent, et al.
Journal of Medical Genetics|July 5, 2003
Visceral manifestations in hereditary haemorrhagic telangiectasia type 2S A Abdalla, U W Geisthoff, D Bonneau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1995
[Early manifestations of Tangier disease]A Lachaux, A Sassolas, R Bouvier, et al.
American Journal of Hematology|April 1, 1988
Asymptomatic association of hemoglobin Dunn (alpha 6[A4]Asp----Asn) and hemoglobin O-Arab (beta 121[GH4]Glu----Lys) in a Moroccan manF Baklouti, A Francina, E Dorléac, et al.
Pediatric Dermatology|March 18, 2000
Elastin gene deletions in Williams syndrome patients result in altered deposition of elastic fibers in skin and a subclinical dermal phenotypeZ Urbán, S Peyrol, H Plauchu, et al.
Human Genetics|March 1, 1997
An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostosesL Legeai-Mallet, P Margaritte-Jeannin, M Lemdani, et al.
Pageof 12

Showing results (81-90 of 116) with videos related to

Sort By:
Pageof 12
Neurology|December 10, 2008
Stroke following pulmonary arteriovenous fistula embolization in a patient with HHTS Felix, S Jeannin, C Goizet, et al.
Radiology|January 1, 1985
Small, asymptomatic angiomyolipomas of the kidneyP M Bret, M Bretagnolle, D Gaillard, et al.
Nature|June 10, 1998
Connexin 26 gene linked to a dominant deafnessF Denoyelle, G Lina-Granade, H Plauchu, et al.
Gastroenterology|December 31, 1998
Liver transplantation resolves the hyperdynamic circulation in hereditary hemorrhagic telangiectasia with hepatic involvementO Boillot, F Bianco, J P Viale, et al.
Pediatrie|April 1, 1975
[Triploidy in the child. I. Study of phenotype. An observation of triploidy with mosaicism 46, XX/69, XXY]M David, A Chambon, C Laurent, et al.
Journal of Medical Genetics|July 5, 2003
Visceral manifestations in hereditary haemorrhagic telangiectasia type 2S A Abdalla, U W Geisthoff, D Bonneau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1995
[Early manifestations of Tangier disease]A Lachaux, A Sassolas, R Bouvier, et al.
American Journal of Hematology|April 1, 1988
Asymptomatic association of hemoglobin Dunn (alpha 6[A4]Asp----Asn) and hemoglobin O-Arab (beta 121[GH4]Glu----Lys) in a Moroccan manF Baklouti, A Francina, E Dorléac, et al.
Pediatric Dermatology|March 18, 2000
Elastin gene deletions in Williams syndrome patients result in altered deposition of elastic fibers in skin and a subclinical dermal phenotypeZ Urbán, S Peyrol, H Plauchu, et al.
Human Genetics|March 1, 1997
An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostosesL Legeai-Mallet, P Margaritte-Jeannin, M Lemdani, et al.
Pageof 12