Works matching DE "CONSANGUINITY"

Results: 1749
    1

    Consanguinity as a Risk Factor for Autism.

    Published in:
    Journal of Autism & Developmental Disorders, 2025, v. 55, n. 6, p. 1945, doi. 10.1007/s10803-023-06137-w
    By:
    • Alshaban, Fouad A.;
    • Aldosari, Mohammad;
    • Ghazal, Iman;
    • Al-Shammari, Hawraa;
    • ElHag, Saba;
    • Thompson, I. Richard;
    • Bruder, Jennifer;
    • Shaath, Hibah;
    • Al-Faraj, Fatema;
    • Tolefat, Mohamed;
    • Nasir, Assal;
    • Fombonne, Eric
    Publication type:
    Article
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    Costs of consanguinity.

    Published in:
    Nature, 1994, v. 371, n. 6498, p. 630, doi. 10.1038/371630a0
    By:
    • Davies, Kevin
    Publication type:
    Article
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    A Case of Consanguinity.

    Published in:
    Global Pediatric Health, 2022, p. 1, doi. 10.1177/2333794X221135965
    By:
    • Brown, Carla;
    • Jones-Brooks, Paige;
    • White, Gwenevere;
    • Shearer, Zackary;
    • Baber, Megan
    Publication type:
    Article
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    Genetic screening of an endemic mutation in the DYSF gene in an isolated, mountainous population in the Republic of Dagestan.

    Published in:
    Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 10, p. 1, doi. 10.1002/mgg3.2236
    By:
    • Bardakov, Sergey N.;
    • Deev, Roman V.;
    • Isaev, Аrtur А.;
    • Khromov‐Borisov, Nikita N.;
    • Kopylov, Evgeniy D.;
    • Savchuk, Мaria R.;
    • Pushkin, Maxim S.;
    • Presnyakov, Evgeniy V.;
    • Magomedova, Raisat M.;
    • Achmedova, Patimat G.;
    • Umakhanova, Zoya R.;
    • Kaimonov, Vladimir S.;
    • Musatova, Elizaveta V.;
    • Blagodatskikh, Konstantin А.;
    • Tveleneva, Aleksandra А.;
    • Sofronova, Yana V.;
    • Yakovlev, Ivan A.
    Publication type:
    Article
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    Spinal muscular atrophy carrier frequency in Saudi Arabia.

    Published in:
    Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 11, p. 1, doi. 10.1002/mgg3.2049
    By:
    • Al Jumah, Mohammed;
    • Al Rajeh, Saad;
    • Eyaid, Wafaa;
    • Al‐Jedai, Ahmed;
    • Al Mudaiheem, Hajar;
    • Al Shehri, Ali;
    • Hussein, Mohammed;
    • Al Abdulkareem, Ibrahim
    Publication type:
    Article
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    Mutation spectrum of congenital heart disease in a consanguineous Turkish population.

    Published in:
    Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 6, p. 1, doi. 10.1002/mgg3.1944
    By:
    • Dong, Weilai;
    • Kaymakcalan, Hande;
    • Jin, Sheng Chih;
    • Diab, Nicholas S.;
    • Tanıdır, Cansaran;
    • Yalcin, Ali Seyfi Yalim;
    • Ercan‐Sencicek, A. Gulhan;
    • Mane, Shrikant;
    • Gunel, Murat;
    • Lifton, Richard P.;
    • Bilguvar, Kaya;
    • Brueckner, Martina
    Publication type:
    Article
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    Fetal akinesia deformation sequence and massive perivillous fibrin deposition resulting in fetal death in six fetuses from one consanguineous couple, including literature review.

    Published in:
    Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 11, p. 1, doi. 10.1002/mgg3.1827
    By:
    • Tjon, Jill K.;
    • Lakeman, Phillis;
    • van Leeuwen, Elisabeth;
    • Waisfisz, Quinten;
    • Weiss, Marjan M.;
    • Tan‐Sindhunata, Gita M. B.;
    • Nikkels, Peter G. J.;
    • van der Voorn, Patrick J. P.;
    • Salomons, Gajja S.;
    • Burchell, George L.;
    • Linskens, Ingeborg H.;
    • van der Knoop, Bloeme J.;
    • de Vries, Johanna I. P.
    Publication type:
    Article
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