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C Turleau

Showing results (121-130 of 155) with videos related to

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Annales De Genetique|January 1, 1987
From oocyte to embryo: a model, deduced from in vitro fertilization, for natural selection against chromosome abnormalitiesM Plachot, J de Grouchy, A M Junca, et al.
Cancer Genetics and Cytogenetics|August 1, 1982
Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosisC Junien, S Despoisse, C Turleau, et al.
Annales De Genetique|January 1, 1984
Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin)C Turleau, J de Grouchy, F Chavin-Colin, et al.
Genomics|October 1, 1992
Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patientsB Plougastel, P Couillin, V Blanquet, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|May 1, 1990
[Prenatal diagnosis of various hereditary blinding diseases]A Michel-Awad, J Kaplan, M L Briard, et al.
Clinical Genetics|July 1, 1996
Parental origin and mechanisms of formation of three cases of 12p tetrasomyC Turleau, B Simon-Bouy, E Austruy, et al.
Human Genetics|January 1, 1981
Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13C Turleau, J de Grouchy, J L Dufier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 13, 2005
[Microarray CGH: principle and use for constitutional disorders]D Sanlaville, J M Lapierre, A Coquin, et al.
Annales De Genetique|January 1, 1989
Regional mapping of the human renin gene to 1q32 by in situ hybridizationO Cohen-Haguenauer, F Soubrier, N Van Cong, et al.
Pageof 16

Showing results (121-130 of 155) with videos related to

Sort By:
Pageof 16
Annales De Genetique|January 1, 1987
From oocyte to embryo: a model, deduced from in vitro fertilization, for natural selection against chromosome abnormalitiesM Plachot, J de Grouchy, A M Junca, et al.
Cancer Genetics and Cytogenetics|August 1, 1982
Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosisC Junien, S Despoisse, C Turleau, et al.
Annales De Genetique|January 1, 1984
Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin)C Turleau, J de Grouchy, F Chavin-Colin, et al.
Genomics|October 1, 1992
Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patientsB Plougastel, P Couillin, V Blanquet, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|May 1, 1990
[Prenatal diagnosis of various hereditary blinding diseases]A Michel-Awad, J Kaplan, M L Briard, et al.
Clinical Genetics|July 1, 1996
Parental origin and mechanisms of formation of three cases of 12p tetrasomyC Turleau, B Simon-Bouy, E Austruy, et al.
Human Genetics|January 1, 1981
Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13C Turleau, J de Grouchy, J L Dufier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 13, 2005
[Microarray CGH: principle and use for constitutional disorders]D Sanlaville, J M Lapierre, A Coquin, et al.
Annales De Genetique|January 1, 1989
Regional mapping of the human renin gene to 1q32 by in situ hybridizationO Cohen-Haguenauer, F Soubrier, N Van Cong, et al.
Pageof 16