A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short‐lived infant-Reference-Cited by-同舟云学术

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A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short‐lived infant

Published:2020-05-12 Issue:8 Volume:34 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Domínguez María Guadalupe¹,Rivera Horacio¹²,Dávalos‐Pulido Rosa María¹,Dávalos‐Rodríguez Ingrid Patricia¹²

Affiliation:

1. División de Genética CIBO Instituto Mexicano del Seguro Social Guadalajara México

2. Doctorado en Genética Humana CUCS Universidad de Guadalajara Guadalajara México

Funder

Instituto Mexicano del Seguro Social

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.23355

Reference25 articles.

1. Nucleolus organizer regions (NORs) inserted in 6q15

2. Complex distal 10q rearrangement in a girl with mild intellectual disability: Follow up of the patient and review of the literature of non-acrocentric satellited chromosomes

3. Familial t(6;21)(p21.1;p13) translocation associated with male-only sterility

4. Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder

5. Prenatal diagnosis of interstitially satellited 6p

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