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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 syndrome
F Perrotin, G Haddad, A Guichet, et al.
International Journal of Pediatric Otorhinolaryngology
|
September 1, 1986
Choanal atresia and deafness
A 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 family
N 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 family
M 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.
Page
of 10
Search research articles
Search
Showing results (21-30 of 94) with videos related to
Sort By:
Page
of 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 syndrome
F Perrotin, G Haddad, A Guichet, et al.
International Journal of Pediatric Otorhinolaryngology
|
September 1, 1986
Choanal atresia and deafness
A 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 family
N 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 family
M 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.
Page
of 10