A rare case of 1q31.1–q32.1 deletion with congenital heart disease

Author:

Takarada Shinya,Yoshimura Naoki,Yo Niida,Hirono Keiichi

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference6 articles.

1. De novo deletion of 1q31.1-q32.1 in a patient with developmental delay and behavioral disorders;Milani;Cytogenet Genome Res,2012

2. Chromosome 1q31.2q32.1 deletion in an adult male with intellectual disability, dysmorphic features and obesity;Hyder;Clin Dysmorphol,2019

3. A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences;Mrasek;Cytogenet Genome Res,2008

4. Interstitial deletion of the long arm of chromosome 1 (1q 25–32). Clinical and endocrine features with a long term follow-up;Maggio;Minerva Pediatr,2003

5. A new case of interstitial 1q 25.3-32.1 deletion: cytogenetic analysis molecular characterization and ultrasound findings;Libotte;J Prenat Med,2015

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