Phenotype of five patients with Greig syndrome and microdeletion of 7p13

American Journal of Medical Genetics

Volumn 102, Issue 3, 2001, Pages 243-249

  Kroisel, Peter M ^a,b   Petek, Erwin ^a   Wagner, Klaus ^a  

^a Inst of Med Biol and Hum Genet   (Austria)

^b UNIVERSITY OF GRAZ   (Austria)

Author keywords

FISH analysis; Greig cephalopolysyndactyly syndrome (GCPS); Microdeletion; Phenotype genotype correlation

Indexed keywords

ADOLESCENT; ARTICLE; CHROMOSOME 7P; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; CYTOGENETICS; FEMALE; GREIG SYNDROME; HIRSUTISM; HUMAN; HYPERGLYCEMIA; MALE; MYOPATHY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; SEIZURE; SYNDACTYLY;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 7; CRANIOFACIAL ABNORMALITIES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; PHENOTYPE; SYNDACTYLY; SYNDROME; TWINS, MONOZYGOTIC;

EID: 0035882364     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1443     Document Type: Article

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