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 *

98 related articles for article (PubMed ID: 10508987)

  • 1. Genetic counseling for childless women at risk for Duchenne muscular dystrophy.
    Eggers S; Pavanello RC; Passos-Bueno MR; Zatz M
    Am J Med Genet; 1999 Oct; 86(5):447-53. PubMed ID: 10508987
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Carrier screening model for Duchenne muscular dystrophy for women of reproductive age based on a pre-pregnancy birth defect control platform].
    Zheng J; Han S; Ye W; Yao S; Qi M; Chen J; Xu H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 May; 38(5):485-487. PubMed ID: 33974262
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophy.
    Helderman-van den Enden AT; Madan K; Breuning MH; van der Hout AH; Bakker E; de Die-Smulders CE; Ginjaar HB
    Eur J Hum Genet; 2013 Jan; 21(1):21-6. PubMed ID: 22669413
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy].
    Zhao W; Jiang N; Li S; Li JS; Miao Y; Liang SY; Yu DY
    Zhonghua Fu Chan Ke Za Zhi; 2019 Apr; 54(4):226-231. PubMed ID: 31006187
    [No Abstract]   [Full Text] [Related]  

  • 6. Duchenne Muscular Dystrophy: a Survey of Perspectives on Carrier Testing and Communication Within the Family.
    Hayes B; Hassed S; Chaloner JL; Aston CE; Guy C
    J Genet Couns; 2016 Jun; 25(3):443-53. PubMed ID: 26482744
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Knowledge of carrier status and barriers to testing among mothers of sons with Duchenne or Becker muscular dystrophy.
    Bogue L; Peay H; Martin A; Lucas A; Ramchandren S
    Neuromuscul Disord; 2016 Dec; 26(12):860-864. PubMed ID: 27863875
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Survey on genetic counseling and health management for symptomatic and asymptomatic female dystrophinopathy carriers in Japan today].
    Kobayashi M; Ishizaki M; Adachi K; Yonemoto N; Matsumura T; Toyoshima I; Kimura E
    Rinsho Shinkeigaku; 2016 Jun; 56(6):407-12. PubMed ID: 27212674
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis.
    Zampatti S; Mela J; Peconi C; Pagliaroli G; Carboni S; Barrano G; Zito I; Cascella R; Marella G; Milano F; Arcangeli M; Caltagirone C; Novelli A; Giardina E
    Prenat Diagn; 2018 Dec; 38(13):1096-1102. PubMed ID: 30303263
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades?
    McGowan R; Challoner BR; Ross S; Holloway S; Joss S; Wilcox D; Holden ST; Tolmie J; Longman C
    Clin Genet; 2013 Feb; 83(2):187-90. PubMed ID: 22428906
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Carrier detection and genetic counselling in Duchenne muscular dystrophy: a follow-up study.
    Hutton EM; Thompson MW
    Can Med Assoc J; 1976 Oct; 115(8):749-52. PubMed ID: 974964
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Joint SOGC-CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing.
    Wilson RD; De Bie I; Armour CM; Brown RN; Campagnolo C; Carroll JC; Okun N; Nelson T; Zwingerman R; Audibert F; Brock JA; Brown RN; Campagnolo C; Carroll JC; De Bie I; Johnson JA; Okun N; Pastruck M; Vallée-Pouliot K; Wilson RD; Zwingerman R; Armour C; Chitayat D; De Bie I; Fernandez S; Kim R; Lavoie J; Leonard N; Nelson T; Taylor S; Van Allen M; Van Karnebeek C
    J Obstet Gynaecol Can; 2016 Aug; 38(8):742-762.e3. PubMed ID: 27638987
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Carrier testing of children for two X-linked diseases: A retrospective study of comprehension of the test results and social and psychological significance of the testing.
    Järvinen O; Lehesjoki AE; Lindlöf M; Uutela A; Kääriäinen H
    Pediatrics; 2000 Dec; 106(6):1460-5. PubMed ID: 11099604
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The value of deletion analysis for carrier detection in Duchenne muscular dystrophy (DMD).
    Bejjani B; Finn P; Milunsky A; Amos J
    Clin Genet; 1991 Apr; 39(4):245-52. PubMed ID: 2070545
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Preimplantation genetic diagnosis associated to Duchenne muscular dystrophy.
    Bianco B; Christofolini DM; Conceição GS; Barbosa CP
    Einstein (Sao Paulo); 2017; 15(4):489-491. PubMed ID: 28954035
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.
    Hodgson S; Walker A; Cole C; Hart K; Johnson L; Heckmatt J; Dubowitz V; Bobrow M
    J Med Genet; 1987 Mar; 24(3):152-9. PubMed ID: 3572997
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?
    Helderman-van den Enden AT; van den Bergen JC; Breuning MH; Verschuuren JJ; Tibben A; Bakker E; Ginjaar HB
    Clin Genet; 2011 Mar; 79(3):236-42. PubMed ID: 21070212
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mosaicism in carrier of Duchenne muscular dystrophy mutation - Implication for prenatal diagnosis.
    Dinh LT; Nguyen DH; Luong LH; Le PT; Le-Anh TP; Tran DQ; Tran TH; Bui TH; Van Ta T; Tran VK
    Taiwan J Obstet Gynecol; 2018 Dec; 57(6):878-880. PubMed ID: 30545545
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comparison of serum creatine kinase estimation with short tandem repeats based linkage analysis in carriers and affected children of Duchenne muscular dystrophy.
    Hashim R; Shaheen S; Ahmad S; Sattar A; Khan FA
    J Ayub Med Coll Abbottabad; 2011; 23(1):125-8. PubMed ID: 22830166
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnosis and management of Duchenne muscular dystrophy in a developing country over a 10-year period.
    Thong MK; Bazlin RI; Wong KT
    Dev Med Child Neurol; 2005 Jul; 47(7):474-7. PubMed ID: 15991868
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.