Partial Trisomy 13 Plus Partial Trisomy 4q Due to Unusual Segregation of Translocation Chromosomes

Overview

Journal Clin Genet

Specialty Genetics

Date 1979 Feb 1

PMID 761418

Citations 6

Authors

C Fonatsch

S D Flatz

E Weitzel

Affiliations

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Abstract

The cytogenetic analysis of a 7-month-old retarded girl with clinical signs compatible with partial trisomy 13 revealed a translocation t(4;13)(q33;q14) and an additional derivative chromosome 13. This karyotype probably resulted from 3:1 segregation during meiosis of the patient's mother.

Citing Articles

Complex balanced translocation of chromosomes 2, 3, and 13.

Muneer R, Donaldson D, Rennert O Hum Genet. 1981; 59(2):182-4.

PMID: 7327579 DOI: 10.1007/BF00293074.

Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three members.

Gilgenkrantz S, Defeche C, STEHLIN S, Gregoire M Hum Genet. 1981; 58(4):436-40.

PMID: 7327568 DOI: 10.1007/BF00282833.

Nondisjunction of a translocation-chromosome t(4;13).

Westmeier M, Kaiser P, Steuber E, KORVER G, Ribhegge I Hum Genet. 1981; 59(4):337-41.

PMID: 6949856 DOI: 10.1007/BF00295467.

Familial translocation leading to partial trisomy 13: report of three cases.

Tharapel S, Lewandowski Jr R, Kukolich M Indian J Pediatr. 1984; 51(411):481-7.

PMID: 6526455 DOI: 10.1007/BF02776437.

Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13.

Tharapel S, Lewandowski R, Tharapel A, Wilroy Jr R J Med Genet. 1986; 23(4):310-5.

PMID: 3746829 PMC: 1049695. DOI: 10.1136/jmg.23.4.310.