Partial trisomy 6p due to maternal t(1;6) translocation

Clinical Genetics

Volumn 49, Issue 6, 1996, Pages 316-317

  Song, Minghao ^a,b   Li, Luyun ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b NONE   (United States)

Author keywords

Congenital anomalies; Mental retardation; Partial trisomy 6p; Reciprocal translocation

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 6P; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION; CONGENITAL MALFORMATION; FEMALE; HUMAN; HUMAN CELL; MENTAL DEFICIENCY; PARTIAL TRISOMY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL;

EID: 0029836020     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb03797.x     Document Type: Article

References (4)

1. Burd L, Martsolf JT, Kerbeshian J, Jalal SM. Partial 6p trisomy associated with infantile autism. Clin Genet 1988: 33: 356-359.
2. Eden MS, James WT, Karen M, Joyce AM. Partial trisomy 6p and partial monosomy 9p from a de novo translocation 46,XY,-9,+der(9)t(6:9)(p21:p24). Clin Genet 1985: 28: 375-384.
3. Scarbrough PR, Carroll AJ, Finley SC, Hamerick K. Partial trisomy 6p and partial trisomy 22 from 3:1 meiotic disjunction of maternal (6p;22q) translocation. J Med Genet 1986: 23: 185-187.
4. Therkelsen AJ, Klinge T, Hinningsen K, Mikkelsen M, Schmidt G. A family with a presumptive C/F translocation in five generations. Ann Genet 1971: 14: 13-21.