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M F Croquette

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

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 16, 1998
[Jejunal atresia and persistent mullerian duct syndrome]S Klosowski, A Abriak, C Morisot, et al.
Human Genetics|March 7, 1998
Y-autosome translocation and infertility: usefulness of molecular, cytogenetic and meiotic studiesB Delobel, R Djlelati, O Gabriel-Robez, et al.
Human Genetics|October 1, 1996
Molecular mapping of a Yq deletion in a patient with normal statureR Rousseaux-Prévost, J M Rigot, B Delobel, et al.
American Journal of Human Genetics|December 1, 1993
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial casesC Desmaze, M Prieur, F Amblard, et al.
Human Molecular Genetics|October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR geneC Vincent, V Kalatzis, S Compain, et al.
Journal of Medical Genetics|October 21, 1999
Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndromeS Manouvrier-Hanu, J Amiel, S Jacquot, et al.
Human Genetics|July 1, 1995
Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literatureS Demczuk, A Lévy, M Aubry, et al.
American Journal of Human Genetics|July 1, 1995
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 regionZ Chettouh, M F Croquette, B Delobel, et al.
The New England Journal of Medicine|December 12, 1991
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardationF Rousseau, D Heitz, V Biancalana, et al.
British Journal of Cancer|June 11, 1999
Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT familiesN Janin, N Andrieu, K Ossian, et al.
Pageof 5

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

Sort By:
Pageof 5
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 16, 1998
[Jejunal atresia and persistent mullerian duct syndrome]S Klosowski, A Abriak, C Morisot, et al.
Human Genetics|March 7, 1998
Y-autosome translocation and infertility: usefulness of molecular, cytogenetic and meiotic studiesB Delobel, R Djlelati, O Gabriel-Robez, et al.
Human Genetics|October 1, 1996
Molecular mapping of a Yq deletion in a patient with normal statureR Rousseaux-Prévost, J M Rigot, B Delobel, et al.
American Journal of Human Genetics|December 1, 1993
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial casesC Desmaze, M Prieur, F Amblard, et al.
Human Molecular Genetics|October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR geneC Vincent, V Kalatzis, S Compain, et al.
Journal of Medical Genetics|October 21, 1999
Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndromeS Manouvrier-Hanu, J Amiel, S Jacquot, et al.
Human Genetics|July 1, 1995
Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literatureS Demczuk, A Lévy, M Aubry, et al.
American Journal of Human Genetics|July 1, 1995
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 regionZ Chettouh, M F Croquette, B Delobel, et al.
The New England Journal of Medicine|December 12, 1991
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardationF Rousseau, D Heitz, V Biancalana, et al.
British Journal of Cancer|June 11, 1999
Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT familiesN Janin, N Andrieu, K Ossian, et al.
Pageof 5