Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): Evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

Journal of Medical Genetics

Volumn 34, Issue 3, 1997, Pages 177-183

  Des Portes, V ^a   Pinard, J M ^b   Smadja, D ^c   Motte, J ^d   Boespflug Tanguy O ^f   Moutard, M L ^e   Desguerre, I ^e   Billuart, P ^a   Carrie, A ^a   Bienvenu, T ^a   Vinet, M C ^a   Bachner, L ^g   Beldjord, C ^a   Dulac, O ^e   Kahn, A ^a   Ponsot, G ^e   Chelly, J ^a  

^a INSTITUT COCHIN   (France)

^b RAYMOND POINCARÉ HOSPITAL   (France)

^c Service de Neurologie   (Martinique)

^d AMERICAN MEMORIAL HOSPITAL   (France)

^e HÔPITAL SAINT VINCENT DE PAUL   (France)

^f INSERM   (France)

^g GIS Infobiogen   (France)

Author keywords

Lissencephaly; Subcortical laminar heterotopia; X inheritance

Indexed keywords

AGYRIA; ARTICLE; BRAIN DEVELOPMENT; CHROMOSOME BREAKAGE; CHROMOSOME XQ; CLINICAL ARTICLE; EPILEPSY; GENE MAPPING; HAPLOTYPE; HETEROTOPIA; HUMAN; MALE; MENTAL DEFICIENCY; MOSAICISM; PRIORITY JOURNAL; X CHROMOSOME DOMINANT INHERITANCE;

EID: 16944367121     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.34.3.177     Document Type: Article

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