Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3.

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Bibliographic Details
Title: Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3.
Authors: Dutta D; Division of Hematology/Oncology, Department of Medicine, SUNY Upstate Medical University, Syracuse, New York, USA duttad@upstate.edu gargri@upstate.edu., Black J; Center of Development, Behavior, and Genetics, SUNY Upstate Medical University, Syracuse, New York, USA., Montoya EA; Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA., Burrow TA; Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA., Shieh J; Division of Medical Genetics, Department of Pediatrics, University of California San Francisco, San Francisco, California, USA., McGivern B; GeneDx, Gaithersburg, Maryland, USA., Raymond M; GeneDx, Gaithersburg, Maryland, USA., Sheedy CB; GeneDx, Gaithersburg, Maryland, USA., Smith SC; Department of Pathology, SUNY Upstate Medical University, Syracuse, New York, USA., Garg R; Center of Development, Behavior, and Genetics, SUNY Upstate Medical University, Syracuse, New York, USA duttad@upstate.edu gargri@upstate.edu.
Source: Journal of medical genetics [J Med Genet] 2025 Mar 20; Vol. 62 (4), pp. 268-275. Date of Electronic Publication: 2025 Mar 20.
Publication Type: Journal Article
Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1468-6244
DOI:10.1136/jmg-2024-110367