Developmental delay, intellectual disability, short stature, subglottic stenosis, hearing impairment, onychodysplasia of the index fingers, and distinctive facial features: A newly reported autosomal recessive syndrome
- DOI
- 10.1002/ajmg.a.61730
- Published
- 2020-07-02
- Container
- American Journal of Medical Genetics Part A
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/ajmg.a.61730,
title = {Developmental delay, intellectual disability, short stature, subglottic stenosis, hearing impairment, onychodysplasia of the index fingers, and distinctive facial features: A newly reported autosomal recessive syndrome},
author = {André Mégarbané and Sayeeda Hana and Stephany El‐Hayek and Alicia Gambarini and Mahmoud Taleb Al‐Ali and Valérie Delague},
year = {2020},
journal = {American Journal of Medical Genetics Part A},
doi = {10.1002/ajmg.a.61730},
url = {https://doi.org/10.1002/ajmg.a.61730}
}RIS
TY - JOUR TI - Developmental delay, intellectual disability, short stature, subglottic stenosis, hearing impairment, onychodysplasia of the index fingers, and distinctive facial features: A newly reported autosomal recessive syndrome AU - André Mégarbané AU - Sayeeda Hana AU - Stephany El‐Hayek AU - Alicia Gambarini AU - Mahmoud Taleb Al‐Ali AU - Valérie Delague PY - 2020 JO - American Journal of Medical Genetics Part A DO - 10.1002/ajmg.a.61730 UR - https://doi.org/10.1002/ajmg.a.61730 ER -
APA
Mégarbané, A., Hana, S., El‐Hayek, S., Gambarini, A., Al‐Ali, M. T., & Delague, V. (2020). Developmental delay, intellectual disability, short stature, subglottic stenosis, hearing impairment, onychodysplasia of the index fingers, and distinctive facial features: A newly reported autosomal recessive syndrome. American Journal of Medical Genetics Part A. https://doi.org/10.1002/ajmg.a.61730
Source records
- crossref · retrieved 2026-09-26T11:41:29.972Z