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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 6, 2024. (Total: 232244Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Cleft Palate and COL2A1[original query]
Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.
Birth defects research. Part A, Clinical and molecular teratology 2010 Sep 88 (9): 748-56.
Nikopensius Tiit, Jagomägi Triin, Krjutskov Kaarel, Tammekivi Veronika, Saag Mare, Prane Inga, Piekuse Linda, Akota Ilze, Barkane Biruta, Krumina Astrida, Ambrozaityte Laima, Matuleviciene Ausra, Kucinskiene Zita Ausrele, Lace Baiba, Kucinskas Vaidutis, Metspalu Andr
Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate.
Birth defects research. Part A, Clinical and molecular teratology 2011 Apr 91 (4): 218-25.
Nikopensius Tiit, Kempa Inga, Ambrozaityt? Laima, Jagomägi Triin, Saag Mare, Matulevi?ien? Aušra, Utkus Algirdas, Krjutškov Kaarel, Tammekivi Veronika, Piekuse Linda, Akota Ilze, Barkane Biruta, Krumina Astrida, Klovins Janis, Lace Baiba, Ku?inskas Vaidutis, Metspalu Andr
Association Between Genes Involved in Craniofacial Development and Nonsyndromic Cleft Lip and/or Palate in the Brazilian Population.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2015 Sep .
Machado Renato Assis, Messetti Ana Camila, de Aquino Sibele Nascimento, Martelli-Júnior Hercílio, Swerts Mário Sérgio Oliveira, de Almeida Reis Silvia Regina, Moreira Helenara Salvati Bertolossi, Persuhn Darlene Camati, Coletta Ricardo
Ophthalmic and molecular genetic findings in Kniest dysplasia.
Eye (London, England) 2015 Apr 29 (4): 475-82.
Sergouniotis P I, Fincham G S, McNinch A M, Spickett C, Poulson A V, Richards A J, Snead M
Novel COL2A1 variants in Japanese patients with spondyloepiphyseal dysplasia congenita.
Human genome variation 2022 5 9 (1): 16.
Akahira-Azuma Moe, Enomoto Yumi, Nakamura Naoyuki, Yokoi Takayuki, Minatogawa Mari, Harada Noriaki, Tsurusaki Yoshinori, Kurosawa Ken
Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing Study.
Frontiers in genetics 2022 3 13 828534.
Lace Baiba, Pajusalu Sander, Livcane Diana, Grinfelde Ieva, Akota Ilze, Mauli?a Ieva, Bark?ne Biruta, Stavusis Janis, Inashkina In
Mutation survey in Taiwanese patients with Stickler syndrome.
Taiwan journal of ophthalmology 2023 1 12 (4): 423-429.
Huang Faye, Wang Tzu-Jou, Cho Wan-Hua, Chen Yi-Hao, Wu Pei-Chang, Kuo Hsi-Ku
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