Paternal balanced reciprocal translocation t(9;22)(q34.3;q11.2) resulting in an lnfant with features of the 9q subtelomere and the 22q11 deletion syndromes due to 3:1 meiotic segregation and tertiary monosomy-Reference-Cited by-同舟云学术

Paternal balanced reciprocal translocation t(9;22)(q34.3;q11.2) resulting in an lnfant with features of the 9q subtelomere and the 22q11 deletion syndromes due to 3:1 meiotic segregation and tertiary monosomy

Published:2009-11 Issue:11 Volume:149A Page:2538-2542
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

McGoey Robin R.,Lacassie Yves

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33078/fullpdf

Reference20 articles.

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2. Viability thresholds for partial trisomies and monosomies. A study of 1,159 viable unbalanced reciprocal translocations;Cohen;Hum Genet,1994

3. A deletion in chromosome 22 can cause DiGeorge syndrome;de la Chapelle;Hum Genet,1981

4. Discussion on a new concept of the cellular basis of immunology;DiGeorge;J Pediatr,1965

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1. A Systematic Review of Reproductive Counseling in Cases of Parental Constitutional Reciprocal Translocation (9;22) Mimicking BCR-ABL1;Frontiers in Genetics;2022-08-04

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4. De novo unbalanced translocation t(15;22)(q26.2;q12) with velo‑cardio‑facial syndrome: A case report and review of the literature;Experimental and Therapeutic Medicine;2018-08-16

5. 22q11.2 Deletion Syndrome due to a Translocation t(6;22) in a Patient Conceived via in vitro Fertilization;Molecular Syndromology;2015-11-14