Associated Papers
Copy number variants suggest different molecular pathways for the pathogenesis of bladder exstrophy.
Nordenskjöld A et al.
American Journal of Medical Genetics. Part A, 2023
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish.
Baranowska Körberg I et al.
Human Molecular Genetics, 2015
Association of WNT9B Gene Polymorphisms With Nonsyndromic Cleft Lip With or Without Cleft Palate in Brazilian Nuclear Families.
Fontoura C et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2015
A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice.
Maupin KA et al.
Bone Research, 2013
Studies with Wnt genes and nonsyndromic cleft lip and palate.
Menezes R et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2010
[Association of muscle segment homeobox gene 1 polymorphisms with nonsyndromic cleft lip with or without cleft palate].
Zhang L et al.
Hua Xi Kou Qiang Yi Xue Za Zhi = Huaxi Kouqiang Yixue Zazhi = West China Journal of Stomatology, 2008
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family.
Niemann S et al.
American Journal of Human Genetics, 2004
The mutation load in an African population. I. An analysis of consanguineous marriages in Nigeria.
Scott-Emuakpor AB
American Journal of Human Genetics, 1974
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