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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 36455867)

  • 21. Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.
    Hussein N; Henneman L; Kai J; Qureshi N
    Cochrane Database Syst Rev; 2021 Oct; 10(10):CD010849. PubMed ID: 34634131
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Heterozygous carriers of Nijmegen Breakage Syndrome have a distinct gene expression phenotype.
    Cheung VG; Ewens WJ
    Genome Res; 2006 Aug; 16(8):973-9. PubMed ID: 16809669
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A Case Report of an Infant with Autosomal Recessive Dystrophic Epidermolysis Bullosa: COL7A1 Gene Mutations at C2005T and G7922A.
    Liu J; Wang L
    Acta Dermatovenerol Croat; 2021 Dec; 29(3):164-166. PubMed ID: 34990346
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Assessment the carrier frequency of monogenic diseases in populations requiring assisted reproductive technology.
    Xu X; He S; Li G; Wang Z; Lv L; Zhao Z; Li Q; Shi B; Hao GM
    BMC Med Genomics; 2024 Aug; 17(1):214. PubMed ID: 39160549
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Counseling for personal health implications identified during reproductive genetic carrier screening.
    Gbur S; Mauney L; Gray KJ; Wilkins-Haug L; Guseh S
    Prenat Diagn; 2021 Oct; 41(11):1460-1466. PubMed ID: 34426984
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Assessing the barriers to cardiac care in carriers of Duchenne and Becker muscular dystrophy.
    Eekhoff L; Edwards J; Martin A; Prijoles EJ
    J Genet Couns; 2019 Oct; 28(5):993-1002. PubMed ID: 31373078
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comprehensive genetic analysis of 961 unrelated Duchenne Muscular Dystrophy patients: Focus on diagnosis, prevention and therapeutic possibilities.
    Kumar SH; Athimoolam K; Suraj M; Das Christu Das MS; Muralidharan A; Jeyam D; Ashokan J; Karthikeyan P; Krishna R; Khanna-Gupta A; Bremadesam Raman L
    PLoS One; 2020; 15(6):e0232654. PubMed ID: 32559196
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The Use of Expanded Carrier Screening in Reproductive Medicine: Scientific Impact Paper No. 74.
    Elson J; Drakeley A; Achilli C; Canham N; Kulke C;
    BJOG; 2024 Sep; 131(10):e81-e85. PubMed ID: 38839259
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Experiences of Women Who Have Had Carrier Testing for Duchenne Muscular Dystrophy and Becker Muscular Dystrophy During Adolescence.
    Fraser HG; Redmond RZ; Scotcher DF
    J Genet Couns; 2018 Dec; 27(6):1349-1359. PubMed ID: 29974322
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Expanded carrier screening: a current survey of physician utilization and attitudes.
    Briggs A; Nouri PK; Galloway M; O'Leary K; Pereira N; Lindheim SR
    J Assist Reprod Genet; 2018 Sep; 35(9):1631-1640. PubMed ID: 30069849
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.
    Hussein N; Weng SF; Kai J; Kleijnen J; Qureshi N
    Cochrane Database Syst Rev; 2018 Mar; 3(3):CD010849. PubMed ID: 29537064
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.
    Hussein N; Weng SF; Kai J; Kleijnen J; Qureshi N
    Cochrane Database Syst Rev; 2015 Aug; 2015(8):CD010849. PubMed ID: 26264938
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Expanded carrier screening in Chinese patients seeking the help of assisted reproductive technology.
    Xi Y; Chen G; Lei C; Wu J; Zhang S; Xiao M; Zhang W; Zhang Y; Sun X
    Mol Genet Genomic Med; 2020 Sep; 8(9):e1340. PubMed ID: 32573981
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Interest in and uptake of genetic counseling for preconception carrier screening when offered to predominantly white reproductive-age persons seeking gynecologic care at a single U.S. academic medical center.
    Nesbit CB; Pollack CC; Mascia NS; LaCroix VH; Applebee DM; Bosco AW; Wilkinson-Ryan I; Erekson ED; Evans RH
    J Genet Couns; 2022 Feb; 31(1):109-119. PubMed ID: 34223670
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
    Zhang J; Ma D; Liu G; Wang Y; Liu A; Li L; Luo C; Hu P; Xu Z
    BMC Med Genet; 2019 Nov; 20(1):180. PubMed ID: 31727011
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A homozygous loss-of-function mutation in GP1BB causing variable clinical phenotypes in a family with Bernard-Soulier syndrome.
    Al-Numair N; Ramzan K; Alquait L; Alshehri M; Imtiaz F; Owaidah T
    Blood Coagul Fibrinolysis; 2021 Jul; 32(5):352-355. PubMed ID: 33657022
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Pregnant Women's Perspectives on Expanded Carrier Screening.
    Propst L; Connor G; Hinton M; Poorvu T; Dungan J
    J Genet Couns; 2018 Sep; 27(5):1148-1156. PubMed ID: 29476298
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical Implementation of Expanded Carrier Screening in Pregnant Women at Early Gestational Weeks: A Chinese Cohort Study.
    Shi M; Liauw AL; Tong S; Zheng Y; Leung TY; Chong SC; Cao Y; Lau TK; Choy KW; Chung JPW
    Genes (Basel); 2021 Mar; 12(4):. PubMed ID: 33805278
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Expanded Carrier Screening and the Complexity of Implementation.
    Silver J; Norton ME
    Obstet Gynecol; 2021 Feb; 137(2):345-350. PubMed ID: 33416279
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Carrier screening for 223 monogenic diseases in Chinese population: a multi-center study in 33 104 individuals].
    Hou W; Fu X; Xie X; Zhang C; Bian J; Mao X; Wen J; Luo C; Jin H; Zhu Q; Qi Q; Qian Y; Yuan J; Zhao Y; Yin A; Li S; Jiang Y; Zhang M; Xiao R; Lu Y
    Nan Fang Yi Ke Da Xue Xue Bao; 2024 Jun; 44(6):1015-1023. PubMed ID: 38977330
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.