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 *

159 related articles for article (PubMed ID: 10690861)

  • 21. Prenatal diagnosis of 21-hydroxylase deficiency caused by gene conversion and rearrangements: pitfalls and molecular diagnostic solutions.
    Mao R; Nelson L; Kates R; Miller CE; Donaldson DL; Tang W; Ward K
    Prenat Diagn; 2002 Dec; 22(13):1171-6. PubMed ID: 12478627
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India.
    Dubey S; Tardy V; Chowdhury MR; Gupta N; Jain V; Deka D; Sharma P; Morel Y; Kabra M
    Indian J Med Res; 2017 Feb; 145(2):194-202. PubMed ID: 28639595
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular characterization of 25 Chinese pedigrees with 21-hydroxylase deficiency.
    Yu Y; Wang J; Huang X; Wang Y; Yang P; Li J; Tsuei SH; Shen Y; Fu Q
    Genet Test Mol Biomarkers; 2011 Mar; 15(3):137-42. PubMed ID: 21198393
    [TBL] [Abstract][Full Text] [Related]  

  • 24. CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency.
    Witchel SF; Smith R; Crivellaro CE; Della Manna T; Dichtchekenian V; Setian N; Damiani D
    Hum Genet; 2000 Apr; 106(4):414-9. PubMed ID: 10830908
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese.
    Lee HH; Chao HT; Lee YJ; Shu SG; Chao MC; Kuo JM; Chung BC
    Hum Genet; 1998 Sep; 103(3):304-10. PubMed ID: 9799085
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia: implications for genetic counseling.
    Speiser PW
    Am J Pharmacogenomics; 2001; 1(2):101-10. PubMed ID: 12174671
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Characterisation of CAH alleles with non-radioactive DNA single strand conformation polymorphism analysis of the CYP21 gene.
    Bobba A; Iolascon A; Giannattasio S; Albrizio M; Sinisi A; Prisco F; Schettini F; Marra E
    J Med Genet; 1997 Mar; 34(3):223-8. PubMed ID: 9132494
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees.
    Day DJ; Speiser PW; Schulze E; Bettendorf M; Fitness J; Barany F; White PC
    Hum Mol Genet; 1996 Dec; 5(12):2039-48. PubMed ID: 8968761
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Congenital adrenal hyperplasia: focus on the molecular basis of 21-hydroxylase deficiency.
    Gonçalves J; Friães A; Moura L
    Expert Rev Mol Med; 2007 Apr; 9(11):1-23. PubMed ID: 17466088
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular approaches for the diagnosis of 21-hydroxylase deficiency and congenital adrenal hyperplasia.
    Wedell A
    Clin Lab Med; 1996 Mar; 16(1):125-37. PubMed ID: 8867587
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular analysis of the CYP21A2 gene in Chinese patients with steroid 21-hydroxylase deficiency.
    Ma D; Chen Y; Sun Y; Yang B; Cheng J; Huang M; Zhang J; Zhang J; Hu P; Lin Y; Jiang T; Xu Z
    Clin Biochem; 2014 Apr; 47(6):455-63. PubMed ID: 24503005
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Highly polymorphic XbaI RFLPs of the human 21-hydroxylase genes among Chinese.
    Chen L; Pan X; Shen Y; Chen Z; Zhang Y; Chen R
    J Med Genet; 1992 Apr; 29(4):231-2. PubMed ID: 1349921
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Validation and clinical application of a locus-specific polymerase chain reaction- and minisequencing-based assay for congenital adrenal hyperplasia (21-hydroxylase deficiency).
    Keen-Kim D; Redman JB; Alanes RU; Eachus MM; Wilson RC; New MI; Nakamoto JM; Fenwick RG
    J Mol Diagn; 2005 May; 7(2):236-46. PubMed ID: 15858147
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of heterozygotic carriers of 21-hydroxylase deficiency: sensitivity of ACTH stimulation tests.
    Witchel SF; Lee PA
    Am J Med Genet; 1998 Apr; 76(4):337-42. PubMed ID: 9545098
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene.
    Lekarev O; Tafuri K; Lane AH; Zhu G; Nakamoto JM; Buller-Burckle AM; Wilson TA; New MI
    J Perinatol; 2013 Jan; 33(1):76-8. PubMed ID: 23269230
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Major-histocompatibility-complex gene markers and restriction-fragment analysis of steroid 21-hydroxylase (CYP21) and complement C4 genes in classical congenital adrenal hyperplasia patients in a single population.
    Partanen J; Koskimies S; Sipilä I; Lipsanen V
    Am J Hum Genet; 1989 May; 44(5):660-70. PubMed ID: 2565078
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testing.
    Rumsby G; Massoud AF; Avey C; Brook CG
    J Med Genet; 1996 Sep; 33(9):798-9. PubMed ID: 8880587
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency.
    Lee HH; Lee YJ; Wang YM; Chao HT; Niu DM; Chao MC; Tsai FJ; Lo FS; Lin SJ
    Mol Genet Metab; 2008 Apr; 93(4):450-7. PubMed ID: 18039588
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of molecular defects causing congenital adrenal hyperplasia by cloning and differential hybridization of polymerase chain reaction-amplified 21-hydroxylase (CYP21) genes.
    Helmberg A; Tabarelli M; Fuchs MA; Keller E; Dobler G; Schnegg I; Knorr D; Albert E; Kofler R
    DNA Cell Biol; 1992 Jun; 11(5):359-68. PubMed ID: 1605859
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 21-hydroxylase deficiency-induced congenital adrenal hyperplasia in 230 Chinese patients: Genotype-phenotype correlation and identification of nine novel mutations.
    Wang R; Yu Y; Ye J; Han L; Qiu W; Zhang H; Liang L; Gong Z; Wang L; Gu X
    Steroids; 2016 Apr; 108():47-55. PubMed ID: 26804566
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.