A Comprehensive review of genetic skeletal disorders reported from Pakistan: A brief commentary
Author:
Funder
KAIMRC, Riyadh Saudi Arabia
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
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3. Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux;Ain;Eur. J. Med. Genet.,2018
4. Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variant;Ain;J. Med. Genet.,2018
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