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A Moncla

Showing results (1-10 of 51) with videos related to

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Journal of Medical Genetics|March 1, 1995
Blepharophimosis-mental retardation syndrome and terminal deletion of chromosome 3pA Moncla, N Philip, J F Mattei
Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|February 15, 2011
Use of DOP-PCR for amplification and labeling of BAC DNA for FISHS Darouich, C Popovici, C Missirian, et al.
Reproductive Biomedicine Online|May 20, 2005
Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A geneA Girardet, A Moncla, S Hamamah, et al.
American Journal of Medical Genetics|October 1, 1990
Parental origin of del(15)(q11-q13) in Angelman and Prader-Willi syndromesR Zori, C Williams, J F Mattei, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Neuropsychological phenotypes of genetic diseases]M O Livet, M A Cournelle, A Moncla, et al.
Genetical Research|April 1, 1992
Chromosomal localisation of the mouse and human peripherin genesA Moncla, F Landon, M G Mattei, et al.
American Journal of Medical Genetics|February 24, 2001
Fragile X syndrome and 22q11.2 microdeletion in the same sibshipC Missirian, A Moncla, M A Voelckel, et al.
Revue Neurologique|September 16, 1999
[Clinical approach to mental retardation of genetic origin]M O Livet, A Moncla, N Philip, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1997
[Smith-Magenis syndrome]D Lacombe, A Moncla, P Malzac, et al.
Journal of Medical Genetics|July 1, 1992
Cerebrofaciothoracic dysplasia: a new familyN Philip, A Guala, A Moncla, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|March 1, 1995
Blepharophimosis-mental retardation syndrome and terminal deletion of chromosome 3pA Moncla, N Philip, J F Mattei
Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|February 15, 2011
Use of DOP-PCR for amplification and labeling of BAC DNA for FISHS Darouich, C Popovici, C Missirian, et al.
Reproductive Biomedicine Online|May 20, 2005
Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A geneA Girardet, A Moncla, S Hamamah, et al.
American Journal of Medical Genetics|October 1, 1990
Parental origin of del(15)(q11-q13) in Angelman and Prader-Willi syndromesR Zori, C Williams, J F Mattei, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Neuropsychological phenotypes of genetic diseases]M O Livet, M A Cournelle, A Moncla, et al.
Genetical Research|April 1, 1992
Chromosomal localisation of the mouse and human peripherin genesA Moncla, F Landon, M G Mattei, et al.
American Journal of Medical Genetics|February 24, 2001
Fragile X syndrome and 22q11.2 microdeletion in the same sibshipC Missirian, A Moncla, M A Voelckel, et al.
Revue Neurologique|September 16, 1999
[Clinical approach to mental retardation of genetic origin]M O Livet, A Moncla, N Philip, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1997
[Smith-Magenis syndrome]D Lacombe, A Moncla, P Malzac, et al.
Journal of Medical Genetics|July 1, 1992
Cerebrofaciothoracic dysplasia: a new familyN Philip, A Guala, A Moncla, et al.
Pageof 6