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Moraine, C
76  results:
Search for persons X
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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11

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/..
 
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12

Expression des gènes de la déficience mentale:

Moraine, C.
Archives de Pédiatrie.  2 (1995)  - p. S49 , 1995
Link: https://doi.org/10.1016/..
 
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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/..
 
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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/..
 
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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/..
 
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