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A Nivelon

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

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Journal De Genetique Humaine|December 1, 1983
[Homogeneous triploidy in 2 premature infants (69 XXY)]J B Gouyon, A Kamp, G Couillault, et al.
Annales De Genetique|April 24, 1999
Two cases of terminal deletion of chromosome 13: clinical features, conventional and molecular cytogenetic analysisI Luquet, B Favre, N Nadal, et al.
American Journal of Medical Genetics|May 1, 1988
Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysisA Hanauer, Y Alembik, S Gilgenkrantz, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1983
[Congenital generalized cutis laxa]D Lambert, F Beer, C Jeannin-Magnificat, et al.
European Journal of Pediatrics|August 1, 1996
Abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz and the lethal acrodysgenital syndromesV Cormier-Daire, C Wolf, A Munnich, et al.
Clinical Genetics|October 1, 1988
Coffin-Lowry syndrome: a multicenter studyS Gilgenkrantz, P Mujica, P Gruet, 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.
Annales De Pediatrie|January 1, 1990
[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia]S Szpiro-Tapia, J Kaplan, A Pelet, et al.
American Journal of Human Genetics|May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb regionN Dahl, L J Hu, M Chery, et al.
American Journal of Medical Genetics|March 10, 2001
Mazabraud syndrome in two patients: clinical overlap with McCune-Albright syndromeL Faivre, A Nivelon-Chevallier, M L Kottler, et al.
Pageof 5

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

Sort By:
Pageof 5
Journal De Genetique Humaine|December 1, 1983
[Homogeneous triploidy in 2 premature infants (69 XXY)]J B Gouyon, A Kamp, G Couillault, et al.
Annales De Genetique|April 24, 1999
Two cases of terminal deletion of chromosome 13: clinical features, conventional and molecular cytogenetic analysisI Luquet, B Favre, N Nadal, et al.
American Journal of Medical Genetics|May 1, 1988
Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysisA Hanauer, Y Alembik, S Gilgenkrantz, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1983
[Congenital generalized cutis laxa]D Lambert, F Beer, C Jeannin-Magnificat, et al.
European Journal of Pediatrics|August 1, 1996
Abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz and the lethal acrodysgenital syndromesV Cormier-Daire, C Wolf, A Munnich, et al.
Clinical Genetics|October 1, 1988
Coffin-Lowry syndrome: a multicenter studyS Gilgenkrantz, P Mujica, P Gruet, 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.
Annales De Pediatrie|January 1, 1990
[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia]S Szpiro-Tapia, J Kaplan, A Pelet, et al.
American Journal of Human Genetics|May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb regionN Dahl, L J Hu, M Chery, et al.
American Journal of Medical Genetics|March 10, 2001
Mazabraud syndrome in two patients: clinical overlap with McCune-Albright syndromeL Faivre, A Nivelon-Chevallier, M L Kottler, et al.
Pageof 5