Genetic haploinsufficiency as a phenotypic determinant of a deletion 13q syndrome

Pediatric and Developmental Pathology

Volumn 8, Issue 6, 2005, Pages 658-665

  Kasyan, Armen G ^a   Benirschke, Kurt ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Encephalocele; Folliculogenesis; Haploinsufficiency

Indexed keywords

ARTICLE; CASE REPORT; CELL FUNCTION; CHROMOSOME 13; CHROMOSOME ABERRATION; CHROMOSOME DELETION 13; DELETION 13Q SYNDROME; ENCEPHALOCELE; FEMALE; GENE MAPPING; HUMAN; INFANT; MALE; OVARY FOLLICLE DEVELOPMENT; PHENOTYPE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; BRAIN; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 13; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; INFANT, NEWBORN; MALE; OVARY;

EID: 29244467712     PISSN: 10935266     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10024-005-0066-z     Document Type: Article

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