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jubin zhang
(7 results)?
A microdeletion of chromosome 9q33.3 encompasses the entire LMX1B gene in a Chinese family with nail patella syndrome.
Int J Mol Sci. 2014 Nov 5;15(11):20158-68. doi: 10.3390/ijms151120158.
Int J Mol Sci. 2014.
PMID: 25380522
Free PMC article.
R75Q de novo dominant mutation of GJB2 in a Chinese family with hearing loss and palmoplantar keratoderma.
Jiang SJ, Di ZH, Huang D, Zhang JB, Zhang YY, Li SQ, He R.
Jiang SJ, et al.
Int J Pediatr Otorhinolaryngol. 2014 Sep;78(9):1461-6. doi: 10.1016/j.ijporl.2014.06.008. Epub 2014 Jun 16.
Int J Pediatr Otorhinolaryngol. 2014.
PMID: 24975403
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A new mutation in the gene ROR2 causes brachydactyly type B1.
Huang D, Jiang S, Zhang Y, Liu X, Zhang J, He R.
Huang D, et al. Among authors: zhang j.
Gene. 2014 Aug 15;547(1):106-10. doi: 10.1016/j.gene.2014.06.035. Epub 2014 Jun 19.
Gene. 2014.
PMID: 24954533
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