The second case with 47, XY, + 8 [38] / 45, XO [12] karyotype

Turkish Journal of Pediatrics

Volumn 44, Issue 1, 2002, Pages 86-89

  Çoǧulu, Özgür ^a   Tirpan, Cengiz ^a   Özkinay, Ferda ^a   Gündüz, Cumhur ^a   Özkinay, Cihangir ^a  

^a EGE UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

AGENESIS; ARACHNODACTYLY; BLOOD ANALYSIS; BONE AGE; CAMPTODACTYLY; CASE REPORT; CHRONIC OTITIS MEDIA; CONTROLLED STUDY; FACIES; FEMALE; HOSPITAL ADMISSION; HUMAN; HYPERTELORISM; INFANT; KARYOTYPE 45,X; LETTER; MENINGITIS; MENTAL DEFICIENCY; MICROCYTOSIS; MICROGNATHIA; MOTOR RETARDATION; TRISOMY 8;

CHROMOSOMES, HUMAN, PAIR 8; FEMALE; HUMANS; INFANT; KARYOTYPING; MOSAICISM; TRISOMY; TURNER SYNDROME;

EID: 0036166995     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (7)

1. Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions
2. Trisomy-8 syndrome
3. Dermatoglyphics in trisomy 8
4. Renal and urinary tract abnormalities associated with chromosome aberrations
5. Double autosomal/gonosomal mosaic aneuploidy: Study of nondisjunction in two cases with trisomy of chromosome 8
6. Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism