Intersitial deletion of 20p: New candidate region for hirschsprung disease and autism?

American Journal of Medical Genetics

Volumn 71, Issue 3, 1997, Pages 298-304

  Michaelis, R C ^a   Skinner, S A ^a   Deason, R ^a   Skinner, C ^a   Moore, C L ^a   Phelan, M C ^a  

^a GREENWOOD GENETIC CENTER   (United States)

Author keywords

20p ; Autism; Chromosome 20; Hirschsprung disease; Neurocristopathies

Indexed keywords

ALAGILLE SYNDROME; ARTICLE; AUTISM; CASE REPORT; CHROMOSOME 20P; CYTOGENETICS; GENE DELETION; HIRSCHSPRUNG DISEASE; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE 46,XY; KARYOTYPING; PHENOTYPE; PRIORITY JOURNAL;

ALAGILLE SYNDROME; AUTISTIC DISORDER; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 20; FEMALE; GENOMIC IMPRINTING; HEARING LOSS; HIRSCHSPRUNG DISEASE; HUMANS; MALE; PHENOTYPE;

EID: 0030753926     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970822)71:3<298::AID-AJMG10>3.0.CO;2-F     Document Type: Article

References (83)