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J L Taillemite

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Cancer Genetics and Cytogenetics|April 13, 1999
Two new cases of papillary renal cell carcinoma with t(X;1)(p11;q21) in femalesC Pérot, J Bougaran, L Boccon-Gibod, et al.
Human Molecular Genetics|November 1, 1993
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctataD Weil, M F Portnoï, J Levilliers, et al.
Annales De Genetique|December 1, 1977
[Partial trisonomy 22]J L Taillemite, G Baheux-Morlier, J Van den Akker, et al.
Annales De Genetique|January 1, 1986
Meiotic behaviour of familial pericentric inversions of chromosomes 1 and 9M R Guichaoua, O Gabriel-Robez, C Ratomponirina, et al.
Fertility and Sterility|November 1, 1980
Semen analysis in subfertile balanced-translocation carriersD Marmor, J L Taillemite, J Van den Akker, et al.
American Journal of Medical Genetics|August 3, 2001
Pierre Robin sequence and interstitial deletion 2q32.3-q33.2C Houdayer, M F Portnoï, F Vialard, et al.
Lancet (London, England)|May 25, 1985
Chromosome abnormalities after autologous bone marrow transplantation with marrow treated by cyclophosphamide derivativesJ van den Akker, N C Gorin, J P Laporte, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
A new case of a severe clinical phenotype of the cat-eye syndromeT Martin Denavit, V Malan, C Grillon, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1981
[Antenatal diagnosis. 601 chromosome examinations (author's transl)]J L Taillemite, N Le Porrier, N Joye, et al.
Journal of Medical Genetics|April 16, 1999
Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3qM F Portnoï, S Boutchneï, F Bouscarat, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Cancer Genetics and Cytogenetics|April 13, 1999
Two new cases of papillary renal cell carcinoma with t(X;1)(p11;q21) in femalesC Pérot, J Bougaran, L Boccon-Gibod, et al.
Human Molecular Genetics|November 1, 1993
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctataD Weil, M F Portnoï, J Levilliers, et al.
Annales De Genetique|December 1, 1977
[Partial trisonomy 22]J L Taillemite, G Baheux-Morlier, J Van den Akker, et al.
Annales De Genetique|January 1, 1986
Meiotic behaviour of familial pericentric inversions of chromosomes 1 and 9M R Guichaoua, O Gabriel-Robez, C Ratomponirina, et al.
Fertility and Sterility|November 1, 1980
Semen analysis in subfertile balanced-translocation carriersD Marmor, J L Taillemite, J Van den Akker, et al.
American Journal of Medical Genetics|August 3, 2001
Pierre Robin sequence and interstitial deletion 2q32.3-q33.2C Houdayer, M F Portnoï, F Vialard, et al.
Lancet (London, England)|May 25, 1985
Chromosome abnormalities after autologous bone marrow transplantation with marrow treated by cyclophosphamide derivativesJ van den Akker, N C Gorin, J P Laporte, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
A new case of a severe clinical phenotype of the cat-eye syndromeT Martin Denavit, V Malan, C Grillon, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1981
[Antenatal diagnosis. 601 chromosome examinations (author's transl)]J L Taillemite, N Le Porrier, N Joye, et al.
Journal of Medical Genetics|April 16, 1999
Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3qM F Portnoï, S Boutchneï, F Bouscarat, et al.
Pageof 5