Refinement of the chromosome 16 locus for benign familial infantile convulsions

Clinical Genetics

Volumn 67, Issue 6, 2005, Pages 517-525

  Callenbach, P M C ^a,b   van den Boogerd, E H ^b   de Coo, R F M ^c   ten Houten, R ^d   Oosterwijk, J C ^a   Hageman, G ^e   Frants, R R ^b   Brouwer, O F ^a   van den Maagdenberg, A M J M ^b  

^a UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^c ERASMUS MEDICAL CENTER   (Netherlands)

^d Location Alkmaar   (Netherlands)

^e MEDISCH SPECTRUM TWENTE   (Netherlands)

Author keywords

Benign familial infantile convulsions; Chromosome 16p; Epilepsy; Linkage analysis

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BENIGN CHILDHOOD EPILEPSY; CHROMOSOME 16P; CHROMOSOME 19Q; CHROMOSOME 1Q; CHROMOSOME 2Q; CHROMOSOME IDENTIFICATION; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DYSKINESIA; ELECTROENCEPHALOGRAM; FOCAL EPILEPSY; GENE LOCUS; GENETIC HETEROGENEITY; GENOTYPE; HUMAN; LINKAGE ANALYSIS; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PEDIGREE ANALYSIS; PRIORITY JOURNAL; REMISSION;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 16; EPILEPSY, BENIGN NEONATAL; GENETIC MARKERS; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LOD SCORE; PEDIGREE;

EID: 18344384060     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2005.00445.x     Document Type: Article

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