Associated Papers
A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.
Zlotina A et al.
Bmc Medical Genomics, 2020
33218365 (PubMed )
Supplement: 12920_2020_821_MOESM1_ESM.xlsx › Sheet_1
Functional properties of a naturally occurring Trp1200----Ser1200 mutation of the insulin receptor.
Moller DE et al.
Molecular Endocrinology (baltimore, Md.), 1990
Protein tyrosine phosphatase 1B gene polymorphisms and essential hypertension: a case-control study in Chinese population.
Gu P et al.
Journal of Endocrinological Investigation, 0
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