Interstitial 10p11.23-p12.1 microdeletions associated with developmental delay, craniofacial abnormalities, and cryptorchidism

American Journal of Medical Genetics, Part A

Volumn 164, Issue 10, 2014, Pages 2623-2626

  Mroczkowski, Henry J ^a   Arnold, Georgianne ^a   Schneck, Francis X ^a   Rajkovic, Aleksandar ^a,b   Yatsenko, Svetlana A ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF PITTSBURGH   (United States)

Author keywords

10p11.2 deletion; Array CGH; Cryptorchidism; MKX gene; Testis

Indexed keywords

GENOMIC DNA;

ARMC4 GENE; ARTICLE; CASE REPORT; CHILD; CHROMOSOME DELETION; CHROMOSOME DELETION 10P11.23; CHROMOSOME DELETION 10P12.1; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CRANIOFACIAL MALFORMATION; CRYPTORCHISM; DEVELOPMENTAL DISORDER; FAMILY HISTORY; GENE; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE PHENOTYPE CORRELATION; HAPLOINSUFFICIENCY; HOMEOBOX; HUMAN; MALE; MEDICAL HISTORY; MICROARRAY ANALYSIS; MKX GENE; MPP7 GENE; PHYSICAL EXAMINATION; PRESCHOOL CHILD; SEX DIFFERENTIATION; WAC GENE; CHROMOSOME 10; CHROMOSOME DISORDER; FEMALE; GENE DELETION; GENETICS; PHENOTYPE; PROCEDURES;

CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 10; CRANIOFACIAL ABNORMALITIES; CRYPTORCHIDISM; DEVELOPMENTAL DISABILITIES; FEMALE; GENETIC ASSOCIATION STUDIES; HAPLOINSUFFICIENCY; HUMANS; MALE; PHENOTYPE; SEQUENCE DELETION;

EID: 84908249713     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36627     Document Type: Article

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