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Moraine, C
38
results:
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english (28)
french (9)
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1
De novo and inherited mutations in the X-linked gene CLCN4 ..:
DDD Study
;
Palmer, E E
;
Stuhlmann, T
...
Molecular Psychiatry. 23 (2016) 2 - p. 222-230 , 2016
Link:
https://doi.org/10.1038/..
?
2
Twenty-five novel mutations including duplications in the A..:
Moizard, M-P
;
Ronce, N
;
Blesson, S
...
Clinical Genetics. 79 (2011) 3 - p. 243-253 , 2011
Link:
https://doi.org/10.1111/..
?
3
Screening of ARX in mental retardation families: consequenc..:
Poirier, K.
;
Lacombe, D.
;
Gilbert-Dussardier, B.
...
Neurogenetics. 7 (2005) 1 - p. 39-46 , 2005
Link:
https://doi.org/10.1007/..
?
4
Oligophrenin 1 mutations frequently cause X-linked mental r..:
Zanni, G.
;
Saillour, Y.
;
Nagara, M.
...
Neurology. 65 (2005) 9 - p. 1364-1369 , 2005
Link:
https://doi.org/10.1212/..
?
5
Déficiences mentales liées au chromosome X : un continuum d..:
des Portes, V
;
Moraine, C
Archives de Pédiatrie. 11 (2004) 6 - p. 569-572 , 2004
Link:
https://doi.org/10.1016/..
?
6
Prenatal diagnosis of trisomy 21 by i(21q): a rare case of ..:
Gilardi, J. L.
;
Perrotin, F.
;
Paillet, C.
...
Prenatal Diagnosis. 22 (2002) 10 - p. 856-858 , 2002
Link:
https://doi.org/10.1002/..
?
7
Evaluation De L'impact Psychologique Et Ftnancier Du Depist..:
Caherec, A.
;
Maurage, C.
;
Zabe, C.
...
Archives de Pédiatrie. 6 (1999) - p. S522 , 1999
Link:
https://doi.org/10.1016/..
?
8
Prenatal diagnosis and management of fetal facial clefts:
Fischer, N.
;
Perrotin, F.
;
Tranquart, F.
...
European Journal of Ultrasound. 7 (1998) - p. S37 , 1998
Link:
https://doi.org/10.1016/..
?
9
Twenty-day cerebral and umbilical Doppler monitoring on a g..:
Fignon, A.
;
Salihagic, A.
;
Akoka, S.
...
European Journal of Obstetrics & Gynecology and Reproductive Biology. 66 (1996) 1 - p. 83-86 , 1996
Link:
https://doi.org/10.1016/..
?
10
Recherche de corrélations entre les donnés de la génétique ..:
Moizard, M.P.
;
Billard
;
Berret, F.
...
Archives de Pédiatrie. 3 (1996) 9 - p. 920 , 1996
Link:
https://doi.org/10.1016/..
?
11
Expression des gènes de la déficience mentale:
Moraine, C.
Archives de Pédiatrie. 2 (1995) - p. S49 , 1995
Link:
https://doi.org/10.1016/..
?
12
Developmental aspects of type II lissencephaly: Comparative..:
Gelot, A.
;
Billette de Villemeur, T.
;
Bordarier, C.
...
Acta Neuropathologica. 89 (1995) 1 - p. 72-84 , 1995
Link:
https://doi.org/10.1007/..
?
13
Antibiothérapie chez le nouveau-né. Enquête d'incidence au ..:
Hamed, A.
;
Malvy, D.
;
Borderon, J.C.
...
Médecine et Maladies Infectieuses. 23 (1993) 10 - p. 663-665 , 1993
Link:
https://doi.org/10.1016/..
?
14
Structural rearrangements of chromosome 13 as additional ab..:
Barin, C.
;
Valtat, C.
;
Briault, S.
...
Cancer Genetics and Cytogenetics. 60 (1992) 2 - p. 206-209 , 1992
Link:
https://doi.org/10.1016/..
?
15
X chromosome-linked Kallmann syndrome: stop mutations valid..:
Hardelin, J P
;
Levilliers, J
;
del Castillo, I
...
Proceedings of the National Academy of Sciences. 89 (1992) 17 - p. 8190-8194 , 1992
Link:
https://doi.org/10.1073/..
1-15