Confirmation of the chromosome 8p23.1 euchromatic duplication as a variant with no clinical manifestations [5]

Prenatal Diagnosis

Volumn 19, Issue 2, 1999, Pages 183-184

  O'Malley, D P ^a   Storto, P D ^a  

^a MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; CASE REPORT; CHROMOSOME 8P; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; CLINICAL FEATURE; FEMALE; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; LETTER; MATERNAL AGE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 0032994856     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1097-0223(199902)19:2<183::aid-pd481>3.0.co;2-9     Document Type: Letter

References (3)

1. Barber, J.C.K., Joyce, C.A., Collinson, M.N., Nicholson, J.C., Willatt, L.R., Dyson, H.M., Bateman, M.S., Green, A.J., Yates, J.R.W., Dennis, R.D. (1998). Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance, J. Med. Genet., 35, 491-496.
2. Joyce, C., Collinson, M., Barber, J. (1996). Validation of a subtelomeric probe and its amplification in cytogenetic duplications of 8p with no detectable phenotypic effect, J. Med. Genet., 33, A3.014.
3. Williams, L., Larkins, S., Roberts, E., Davidson, E.V. (1996). Two further cases of variation in band 8p23.1. Not always a benign variant?, J. Med. Genet., 33, A3.020.