Robinow syndrome (RS) is a well‐recognized Mendelian disorder known to demonstrate both autosomal dominant and autosomal recessive inheritance. Typical manifestations include short stature, characteristic facies, and skeletal anomalies. Recessive inheritance has been associated with mutations in
- Award ID(s):
- 1735225
- NSF-PAR ID:
- 10281433
- Date Published:
- Journal Name:
- Genes
- Volume:
- 12
- Issue:
- 2
- ISSN:
- 2073-4425
- Page Range / eLocation ID:
- 151
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.3390/genes12020151
