These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


330 related items for PubMed ID: 30633559

  • 1. Molecular Screening of VAX1 Gene Polymorphisms Uncovered the Genetic Heterogeneity of Nonsyndromic Orofacial Cleft Among Saudi Arabian Patients.
    Sabbagh HJ, Innes NPT, Edris Ahmed S, Butali A, Alnamnakani EA, Rabah SM, Hamdan MA, Alhamlan NH, Abdulhameed FD, Hassan MHA, Al Mahdi HB, Alamoudi NM, Al-Aama JY, Alaki SM, Mossey PA.
    Genet Test Mol Biomarkers; 2019 Jan; 23(1):45-50. PubMed ID: 30633559
    [Abstract] [Full Text] [Related]

  • 2. Polymorphic variants in VAX1 and the risk of nonsyndromic cleft lip with or without cleft palate in a population from northern China.
    Li D, Liu T, Meng X, Guo Q, Shi J, Hao Y, Jiao X, Lv K, Song T.
    Medicine (Baltimore); 2017 Apr; 96(14):e6550. PubMed ID: 28383424
    [Abstract] [Full Text] [Related]

  • 3. The risk of nonsyndromic cleft lip with or without cleft palate and Vax1 rs7078160 polymorphisms in southern Han Chinese.
    Wang Q, Sun S, Song Q, Hu H, An J, Liu J.
    Braz J Otorhinolaryngol; 2021 Apr; 87(6):718-722. PubMed ID: 33132092
    [Abstract] [Full Text] [Related]

  • 4. VAX1 gene associated non-syndromic cleft lip with or without palate in Western Han Chinese.
    Zhang BH, Shi JY, Lin YS, Shi B, Jia ZL.
    Arch Oral Biol; 2018 Nov; 95():40-43. PubMed ID: 30048854
    [Abstract] [Full Text] [Related]

  • 5. Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
    Butali A, Suzuki S, Cooper ME, Mansilla AM, Cuenco K, Leslie EJ, Suzuki Y, Niimi T, Yamamoto M, Ayanga G, Erkhembaatar T, Furukawa H, Fujiwawa K, Imura H, Petrin AL, Natsume N, Beaty TH, Marazita ML, Murray JC.
    Am J Med Genet A; 2013 May; 161A(5):965-72. PubMed ID: 23463464
    [Abstract] [Full Text] [Related]

  • 6. Prevalence and characteristics of non-syndromic orofacial clefts and the influence of consanguinity.
    Alamoudi NM, Sabbagh HJ, Innes NP, El Derwi D, Hanno AZ, Al-Aama JY, Habiballah AH, Mossey PA.
    J Clin Pediatr Dent; 2014 May; 38(3):241-6. PubMed ID: 25095319
    [Abstract] [Full Text] [Related]

  • 7. Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations.
    Gowans LJ, Adeyemo WL, Eshete M, Mossey PA, Busch T, Aregbesola B, Donkor P, Arthur FK, Bello SA, Martinez A, Li M, Augustine-Akpan EA, Deressa W, Twumasi P, Olutayo J, Deribew M, Agbenorku P, Oti AA, Braimah R, Plange-Rhule G, Gesses M, Obiri-Yeboah S, Oseni GO, Olaitan PB, Abdur-Rahman L, Abate F, Hailu T, Gravem P, Ogunlewe MO, Buxó CJ, Marazita ML, Adeyemo AA, Murray JC, Butali A.
    J Dent Res; 2016 Oct; 95(11):1245-56. PubMed ID: 27369588
    [Abstract] [Full Text] [Related]

  • 8. Association between FOXE1 and non-syndromic orofacial clefts in a northeastern Chinese population.
    Liu K, Lu Y, Ai L, Jiao B, Yu J, Zhang B, Liu Q.
    Br J Oral Maxillofac Surg; 2015 Oct; 53(8):705-10. PubMed ID: 26100861
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Birth prevalence of non-syndromic orofacial clefts in Saudi Arabia and the effects of parental consanguinity.
    Sabbagh HJ, Innes NP, Sallout BI, Alamoudi NM, Hamdan MA, Alhamlan N, Al-Khozami AI, Abdulhameed FD, Al-Aama JY, Mossey PA.
    Saudi Med J; 2015 Sep; 36(9):1076-83. PubMed ID: 26318465
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Understanding the participation of GREM1 polymorphisms in nonsyndromic cleft lip with or without cleft palate in the Brazilian population.
    Viena CS, Machado RA, Persuhn DC, Martelli-Júnior H, Medrado AP, Coletta RD, Reis SRA.
    Birth Defects Res; 2019 Jan 01; 111(1):16-25. PubMed ID: 30402937
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 17.