Trisomy 9p Resulting from Maternal 9/21 Translocation

Overview

Journal Hum Genet

Specialty Genetics

Date 1976 May 19

PMID 944684

Citations 6

Authors

I Subrt

B BLEHOVA

B Pallova

Affiliations

Soon will be listed here.

Abstract

The clinical picture found in a child with trisomy 9p confirmed that this chromosomal syndrome is a entity, which arises from maternal translocation t(9;21).

Citing Articles

Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.

Jalbert P, Sele B, Jalbert H Hum Genet. 1980; 55(2):209-22.

PMID: 7450764 DOI: 10.1007/BF00291769.

Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.

Duckett D, Roberts S Hum Genet. 1981; 58(4):377-86.

PMID: 7035334 DOI: 10.1007/BF00282819.

Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings.

Tolksdorf M, Kunze J, Sperling K, Wegner R, Wieczorek V, Vogel M Eur J Pediatr. 1977; 126(1-2):13-27.

PMID: 902660 DOI: 10.1007/BF00443119.

De novo trisomy 9pter leads to q13.

Kardon N, Salwen H, Krauss M, Davis J, Jenkins E Hum Genet. 1977; 37(2):149-53.

PMID: 885535 DOI: 10.1007/BF00393577.

Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

Jalbert P, Sele B J Med Genet. 1979; 16(6):467-78.

PMID: 395305 PMC: 1012595. DOI: 10.1136/jmg.16.6.467.

References

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