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C Moraine

Showing results (21-30 of 94) with videos related to

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Annales De Pediatrie|February 1, 1972
[Cytomeglaic inclusion disease in the newborn. Apropos of 4 cases]C Mercier, C Moraine, J Laugier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1991
[Value of ultrasonic diagnosis of fetal malformations in the detection of chromosomal abnormalities]D Galliano, C Paillet, G Body, et al.
Annales De Pediatrie|September 1, 1992
[Menkes syndrome. An unusual pigmentation anomaly in a mother and three sisters]G Lorette, A Toutain, M Barthes, et al.
Prenatal Diagnosis|June 22, 2000
Prenatal ultrasonographic diagnosis of the popliteal pterygium syndromeF Perrotin, G Haddad, A Guichet, et al.
International Journal of Pediatric Otorhinolaryngology|September 1, 1986
Choanal atresia and deafnessA Robier, M J Ployet, B Loustalot, et al.
Archives Francaises De Pediatrie|March 1, 1989
[Autism and fragile X syndrome. Pedopsychiatric aspects]P Le Louarn, C Moraine, A Perrot, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1991
[X-linked chondrodysplasia punctata: neonatal manifestations]G Lorette, L Vaillant, M C Grangeponte, et al.
American Journal of Human Genetics|July 1, 1997
A C2055T transition in exon 8 of the ATP7A gene is associated with exon skipping in an occipital horn syndrome familyN Ronce, M P Moizard, L Robb, et al.
American Journal of Medical Genetics|March 21, 1998
X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one familyM Raynaud, N Ronce, A D Ayrault, et al.
American Journal of Medical Genetics|November 4, 1998
Are Dp71 and Dp140 brain dystrophin isoforms related to cognitive impairment in Duchenne muscular dystrophy?M P Moizard, C Billard, A Toutain, et al.
Pageof 10

Showing results (21-30 of 94) with videos related to

Sort By:
Pageof 10
Annales De Pediatrie|February 1, 1972
[Cytomeglaic inclusion disease in the newborn. Apropos of 4 cases]C Mercier, C Moraine, J Laugier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1991
[Value of ultrasonic diagnosis of fetal malformations in the detection of chromosomal abnormalities]D Galliano, C Paillet, G Body, et al.
Annales De Pediatrie|September 1, 1992
[Menkes syndrome. An unusual pigmentation anomaly in a mother and three sisters]G Lorette, A Toutain, M Barthes, et al.
Prenatal Diagnosis|June 22, 2000
Prenatal ultrasonographic diagnosis of the popliteal pterygium syndromeF Perrotin, G Haddad, A Guichet, et al.
International Journal of Pediatric Otorhinolaryngology|September 1, 1986
Choanal atresia and deafnessA Robier, M J Ployet, B Loustalot, et al.
Archives Francaises De Pediatrie|March 1, 1989
[Autism and fragile X syndrome. Pedopsychiatric aspects]P Le Louarn, C Moraine, A Perrot, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1991
[X-linked chondrodysplasia punctata: neonatal manifestations]G Lorette, L Vaillant, M C Grangeponte, et al.
American Journal of Human Genetics|July 1, 1997
A C2055T transition in exon 8 of the ATP7A gene is associated with exon skipping in an occipital horn syndrome familyN Ronce, M P Moizard, L Robb, et al.
American Journal of Medical Genetics|March 21, 1998
X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one familyM Raynaud, N Ronce, A D Ayrault, et al.
American Journal of Medical Genetics|November 4, 1998
Are Dp71 and Dp140 brain dystrophin isoforms related to cognitive impairment in Duchenne muscular dystrophy?M P Moizard, C Billard, A Toutain, et al.
Pageof 10