Defective sexual development in an infant with 46, XY, der(9)t(8;9)(q23.1;p23)mat

European Journal of Pediatrics

Volumn 158, Issue 3, 1999, Pages 213-216

  Pfeiffer, R A ^a   Rauch, A ^a   Trautmann, U ^a   Dorr H G ^b   Hiort, O ^c   Scherer, G ^d   Rosch G ^b   Papadopoulos, T ^b   V D Hardt, K ^b   Lachmann, E ^e  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b UNIVERSITY HOSPITAL ERLANGEN   (Germany)

^c Klin fur Padiatrie der Med H   (Germany)

^d UNIVERSITY OF FREIBURG   (Germany)

^e Klinikum Weiden   (Germany)

Author keywords

Defective male sexual morphogenesis; Deletion 9p; Duplication 8q

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 8P; CHROMOSOME DELETION; CRANIOFACIAL MALFORMATION; GENE MUTATION; GENITAL MALFORMATION; HUMAN; HUMAN TISSUE; HYPOSPADIAS; INFANT; MALE; MALE GENITAL SYSTEM; PHENOTYPE; PRIORITY JOURNAL; SEX DETERMINATION; TRISOMY; UROGENITAL SINUS;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 8; CHROMOSOMES, HUMAN, PAIR 9; GENE DUPLICATION; GONADAL DYSGENESIS, 46,XY; HUMANS; INFANT; KARYOTYPING; MALE; TRISOMY;

EID: 0033003575     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310051052     Document Type: Article

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