Cortical periventricular heterotopia with ectodermal dysplasia [1]

American Journal of Medical Genetics

Volumn 113, Issue 4, 2002, Pages 385-389

  Zannolli, Raffaella ^a   Conversano, E ^a   Serracca, L ^a   Di Bartolo, R M ^a   Molinelli, M ^a   Galluzzi, P ^b   Mazzei, M A ^a   Terrosi Vagnoli, P ^a   Miracco, C ^a   De Santi, M M ^a   Vatti, G ^a   Coviello, G ^b   Malandrini, A ^a   Gonnelli, S ^a   Alessandrini, C ^a   Fimiani, M ^a  

^a UNIVERSITY OF SIENA   (Italy)

^b UNIVERSITY HOSPITAL OF SIENA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

FILAMIN; FILAMIN A; FILAMIN C; GLYCINE; UNCLASSIFIED DRUG; ACTIN BINDING PROTEIN; CONTRACTILE PROTEIN; FILAMINS;

BLOOD CLOTTING DISORDER; BRAIN CORTEX; CASE REPORT; CEREBELLAR ATAXIA; CHILD; DUAL ENERGY X RAY ABSORPTIOMETRY; ECTODERMAL DYSPLASIA; ELECTROENCEPHALOGRAM; EPILEPSY; FEMALE; GENE MUTATION; HETEROTOPIA; HETEROZYGOSITY; HUMAN; JOINT LAXITY; LETTER; MALE; MENTAL DEFICIENCY; NUCLEAR MAGNETIC RESONANCE IMAGING; OSTEOPENIA; PATENT DUCTUS ARTERIOSUS; PRIORITY JOURNAL; SKIN BIOPSY; SKIN DEFECT; SPONTANEOUS ABORTION; UROLITHIASIS; X CHROMOSOME DOMINANT DISORDER; CONGENITAL MALFORMATION; FAMILY HEALTH; GENETICS; MULTIPLE MALFORMATION SYNDROME; NERVOUS SYSTEM MALFORMATION; PATHOLOGY; PRESCHOOL CHILD; SYNDROME;

ATAXIA;

ABNORMALITIES, MULTIPLE; CEREBRAL CORTEX; CHILD; CHILD, PRESCHOOL; CONTRACTILE PROTEINS; ECTODERMAL DYSPLASIA; FAMILY HEALTH; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MICROFILAMENT PROTEINS; NERVOUS SYSTEM MALFORMATIONS; SYNDROME;

EID: 12244293057     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.b.10811     Document Type: Letter

References (15)

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