Significance of a prenatally diagnosed del(10)(q23)

American Journal of Medical Genetics

Volumn 107, Issue 2, 2002, Pages 174-176

  Verma, R ^a   Kleyman, S ^a   Sohal, D ^a   Shklooskaya, T ^a   Kazi, R ^a   Jacob, J ^a   Zaslav, A ^a   Allan, S ^a   Fox, J ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

Deletion 10q; Mosaicism; Prenatal diagnosis

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; BLOOD SAMPLING; CASE REPORT; CHROMOSOME 10; CHROMOSOME ANALYSIS; CHROMOSOME MOSAICISM; FEMALE; FOLLOW UP; GENE DELETION; GENETIC COUNSELING; HUMAN; KARYOTYPING; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; STRUCTURAL CHROMOSOME ABERRATION; TISSUE CULTURE;

ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 10; FEMALE; HUMANS; KARYOTYPING; MOSAICISM; PRENATAL DIAGNOSIS;

EID: 0037079988     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10112     Document Type: Article

References (5)

1. Proposed guidelines for diagnosis of mosaicism and pseudomosaicism studied
2. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: A collaborative study
3. Folate sensitive site at 10q23 and its expression as a deletion
4. A rapid banding technique for human chromosomes