HuGE Literature Finder
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| Association between PTCH1 and RAD54B Single-Nucleotide Polymorphisms and Non-syndromic Orofacial Clefts in the Northeast Population of Iran. Avicenna journal of medical biotechnology 2022 12 14 (4): 310-316. Morvaridi Farimani Reza, Azimi-Nezhad Mohsen, KhorramKhorshid Hamid Reza, Ebadifar Asghar, Tohidkhah Saba, Jafarian Zahra, Kamali Koorosh, Nazari Zeinab, Ebrahimzadeh-Vesal Re |
| [Exploring parent-of-origin effects for non-syndromic cleft lip with or without cleft palate on PTCH1, PTCH2, SHH, SMO genes in Chinese case-parent trios]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2020 Oct 52 (5): 809-814. Li W Y, Wang M Y, Zhou R, Wang S Y, Zheng H C, Zhu H P, Zhou Z B, Wu T, Wang H, Shi |
| Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation. Frontiers in genetics 2018 11 9 502. Indencleef Karlijne, Roosenboom Jasmien, Hoskens Hanne, White Julie D, Shriver Mark D, Richmond Stephen, Peeters Hilde, Feingold Eleanor, Marazita Mary L, Shaffer John R, Weinberg Seth M, Hens Greet, Claes Pet |
| Testing reported associations of genetic risk factors for oral clefts in a large Irish study population. Birth defects research. Part A, Clinical and molecular teratology 2010 Feb 88 (2): 84-93. Carter Tonia C, Molloy Anne M, Pangilinan Faith, Troendle James F, Kirke Peadar N, Conley Mary R, Orr David J A, Earley Michael, McKiernan Eamon, Lynn Ena C, Doyle Anne, Scott John M, Brody Lawrence C, Mills James |
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