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B le Marec

Showing results (41-50 of 103) with videos related to

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Journal De Genetique Humaine|December 1, 1983
[Anhidrotic ectodermal dysplasia (apropos of 3 families). Abnormal hair, a sign of heterozygosity?]B Le Marec, M Roussey, J Chevrant-Breton, et al.
Annales De Genetique|January 1, 1985
[Trisomy 20p derived from a maternal pericentric inversion and brachymesophalangy of the index finger]J Lucas, F Le Mée, B Le Marec, et al.
Annales De Genetique|January 1, 1986
46,XX,t(15;21)/47,XX,15p-,+21 mosaicism in a child with Down's syndromeJ Lucas, F Le Mee, K Pluquailec, et al.
Human Genetics|December 1, 1991
Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28V Biancalana, B Le Marec, S Odent, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1986
[Anencephaly and diprosopy: 2 cases]H Journel, P Parent, H Leguern, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1980
[Late prenatal diagnosis of fetal growth retardation: the diagnosis of a case of trisomy 18 (author's transl)]B Le Marec, G Defawe, J E Mention, et al.
Archives Francaises De Pediatrie|January 1, 1988
[Stenosis of the common bile duct on a common biliopancreatic duct]A Dabadie, M Roussey, B Fremond, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephalyL Pasquier, C Dubourg, M Blayau, et al.
Journal De Genetique Humaine|October 1, 1979
[Recessive microencephaly linked to the X chromosome]Y Deshaies, H D Rott, H F Wissmuller, et al.
Presse Medicale (Paris, France : 1983)|September 13, 1986
[Genetic counseling in cancerology]B Le Marec, E Le Gall, H Journel, et al.
Pageof 11

Showing results (41-50 of 103) with videos related to

Sort By:
Pageof 11
Journal De Genetique Humaine|December 1, 1983
[Anhidrotic ectodermal dysplasia (apropos of 3 families). Abnormal hair, a sign of heterozygosity?]B Le Marec, M Roussey, J Chevrant-Breton, et al.
Annales De Genetique|January 1, 1985
[Trisomy 20p derived from a maternal pericentric inversion and brachymesophalangy of the index finger]J Lucas, F Le Mée, B Le Marec, et al.
Annales De Genetique|January 1, 1986
46,XX,t(15;21)/47,XX,15p-,+21 mosaicism in a child with Down's syndromeJ Lucas, F Le Mee, K Pluquailec, et al.
Human Genetics|December 1, 1991
Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28V Biancalana, B Le Marec, S Odent, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1986
[Anencephaly and diprosopy: 2 cases]H Journel, P Parent, H Leguern, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1980
[Late prenatal diagnosis of fetal growth retardation: the diagnosis of a case of trisomy 18 (author's transl)]B Le Marec, G Defawe, J E Mention, et al.
Archives Francaises De Pediatrie|January 1, 1988
[Stenosis of the common bile duct on a common biliopancreatic duct]A Dabadie, M Roussey, B Fremond, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephalyL Pasquier, C Dubourg, M Blayau, et al.
Journal De Genetique Humaine|October 1, 1979
[Recessive microencephaly linked to the X chromosome]Y Deshaies, H D Rott, H F Wissmuller, et al.
Presse Medicale (Paris, France : 1983)|September 13, 1986
[Genetic counseling in cancerology]B Le Marec, E Le Gall, H Journel, et al.
Pageof 11