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 *

173 related articles for article (PubMed ID: 9067760)

  • 21. Molecular analysis of patient and carrier genes with congenital steroid 21-hydroxylase deficiency by using polymerase chain reaction and single strand conformation polymorphism.
    Tajima T; Fujieda K; Nakayama K; Fujii-Kuriyama Y
    J Clin Invest; 1993 Nov; 92(5):2182-90. PubMed ID: 8227333
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical heterogeneity of 21-hydroxylase deficiency of sibs with identical 21-hydroxylase genes.
    Bormann M; Kochhan L; Knorr D; Bidlingmaier F; Olek K
    Acta Endocrinol (Copenh); 1992 Jan; 126(1):7-9. PubMed ID: 1736550
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Who is a carrier? Detection of unsuspected mutations in 21-hydroxylase deficiency.
    Witchel SS; Lee PA; Trucco M
    Am J Med Genet; 1996 Jan; 61(1):2-9. PubMed ID: 8741909
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Screening of CYP21 gene mutations in 129 French patients affected by steroid 21-hydroxylase deficiency.
    Barbat B; Bogyo A; Raux-Demay MC; Kuttenn F; Boué J; Simon-Bouy B; Serre JL; Mornet E
    Hum Mutat; 1995; 5(2):126-30. PubMed ID: 7749410
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Study of a kindred with classic congenital adrenal hyperplasia: diagnostic challenge due to phenotypic variance.
    Chin D; Speiser PW; Imperato-McGinley J; Dixit N; Uli N; David R; Oberfield SE
    J Clin Endocrinol Metab; 1998 Jun; 83(6):1940-5. PubMed ID: 9626123
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Extended MHC haplotypes and CYP21/C4 gene organisation in Irish 21-hydroxylase deficiency families.
    Sinnott PJ; Costigan C; Dyer PA; Harris R; Strachan T
    Hum Genet; 1991 Jul; 87(3):361-6. PubMed ID: 1677925
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Morel Y; Miller WL
    Adv Hum Genet; 1991; 20():1-68. PubMed ID: 1801590
    [No Abstract]   [Full Text] [Related]  

  • 29. Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis.
    Lako M; Ramsden S; Campbell RD; Strachan T
    J Med Genet; 1999 Feb; 36(2):119-24. PubMed ID: 10051010
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Genetic of the 21 hydroxylase deficiency].
    Boué A; Couillin P; Pomarède R; Rappaport R; Boué J
    Ann Endocrinol (Paris); 1982; 43(1):3-14. PubMed ID: 6982657
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype].
    Dumić M; Brkljacić L; Krzisnik C; Radica A; Tajić M; Kastelan A
    Lijec Vjesn; 1983; 105(7-8):290-2. PubMed ID: 6605467
    [No Abstract]   [Full Text] [Related]  

  • 32. Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21B.
    Donohoue PA; Jospe N; Migeon CJ; Van Dop C
    Genomics; 1989 Oct; 5(3):397-406. PubMed ID: 2613228
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Mutation analysis in families with 21-hydroxylase deficiency].
    Wang H; Jiang L; Wang PP; Zhou HB; Wang JL; Song LL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):681-4. PubMed ID: 18067083
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Comprehensive analytical strategy for mutation screening in 21-hydroxylase deficiency.
    Krone N; Roscher AA; Schwarz HP; Braun A
    Clin Chem; 1998 Oct; 44(10):2075-82. PubMed ID: 9761237
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular basis of congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency.
    Simard J; Rhéaume E; Sanchez R; Laflamme N; de Launoit Y; Luu-The V; van Seters AP; Gordon RD; Bettendorf M; Heinrich U
    Mol Endocrinol; 1993 May; 7(5):716-28. PubMed ID: 8316254
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Survival of steroid 21-hydroxylase-deficient mice without endogenous corticosteroids after neonatal treatment and genetic rescue by transgenesis as a model system for treatment of congenital adrenal hyperplasia in humans.
    Gotoh H; Kusakabe M; Shiroishi T; Moriwaki K
    Endocrinology; 1994 Oct; 135(4):1470-6. PubMed ID: 7925109
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: characteristics of three unusual haplotypes.
    Koppens PF; Hoogenboezem T; Degenhart HJ
    Hum Genet; 2002 Oct; 111(4-5):405-10. PubMed ID: 12384784
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phenotypic evolution of classic 21-hydroxylase deficiency.
    Hoffman WH; Shin MY; Donohoue PA; Helman SW; Brown SL; Rosculet G; Mahesh VB
    Clin Endocrinol (Oxf); 1996 Jul; 45(1):103-9. PubMed ID: 8796146
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Layrisse Z; White C; Gunczler P; Gafaro Valera L; Arias S; Yunis EJ; Alper CA; Awdeh ZL
    Immunogenetics; 1987; 25(2):99-103. PubMed ID: 3493216
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients.
    Livieri C; Belvedere M; Martinetti M; Beluffi G; Fiori P; Cogliati CR; Goffredo V; Lorini R; Severi F
    Prog Clin Biol Res; 1985; 200():243-55. PubMed ID: 3001775
    [No Abstract]   [Full Text] [Related]  

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