Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population

ConclusionOur results might suggest that variants influencing GREM1 expression levels, rather than variants affecting the function of the encoded protein, are significant factors in NSCL/P etiology. Birth Defects Research (Part A), 2015. © 2015 Wiley Periodicals, Inc.

Source: Birth Defects Research Part A: Clinical and Molecular Teratology - May 1, 2015 Category: Perinatology & Neonatology Authors: Adrianna Mostowska, Kamil K. Hozyasz, Piotr Wójcicki, Kacper Żukowski, Anna Dąbrowska, Agnieszka Lasota, Małgorzata Zadurska, Agnieszka Radomska, Izabela Dunin‐Wilczyńska, Paweł P. Jagodziński Tags: Original Research Article Source Type: research