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Journal Abstract Search
337 related items for PubMed ID: 3006204
1. [Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis]. Lambotte C. Rev Med Liege; 1986 Jan 15; 41(2):37-44. PubMed ID: 3006204 [No Abstract] [Full Text] [Related]
2. [Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency]. Couillin P. Presse Med; 1984 Apr 21; 13(17):1087-90. PubMed ID: 6232534 [Abstract] [Full Text] [Related]
3. Pitfalls in prenatal diagnosis of 21-hydroxylase deficiency by amniotic fluid steroid analysis? A six years experience in 102 pregnancies at risk. Forest MG. Ann N Y Acad Sci; 1985 Apr 21; 458():130-47. PubMed ID: 3879118 [No Abstract] [Full Text] [Related]
7. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by amniotic fluid steroid analysis. Hughes IA, Laurence KM. Prenat Diagn; 1982 Apr 21; 2(2):97-102. PubMed ID: 6983064 [Abstract] [Full Text] [Related]
8. Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Pang SY, Pollack MS, Marshall RN, Immken L. N Engl J Med; 1990 Jan 11; 322(2):111-5. PubMed ID: 2403652 [No Abstract] [Full Text] [Related]
10. Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes. Raux-Demay M, Mornet E, Boue J, Couillin P, Oury JF, Ravise N, Deluchat C, Boue A. Prenat Diagn; 1989 Jul 11; 9(7):457-66. PubMed ID: 2788885 [Abstract] [Full Text] [Related]
12. Amniotic 17-alpha hydroxyprogesterone and HLA typing for the prenatal diagnosis of 21-alpha hydroxylase deficiency--congenital adrenal hyperplasia. Rosenmann A, Schumert Z, Theodor R, Cohen T, Brautbar C. Am J Med Genet; 1980 Jul 11; 6(4):295-300. PubMed ID: 7211946 [Abstract] [Full Text] [Related]
13. [Neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 2. Analysis of steroids with high-performance liquid chromatography for diagnosis of congenital adrenal hyperplasia]. Mizushima Y, Fukushi M, Arai O, Takasugi N, Fujieda K, Matsuura N, Fujimoto S. Nihon Naibunpi Gakkai Zasshi; 1987 Feb 20; 63(2):102-12. PubMed ID: 3494637 [Abstract] [Full Text] [Related]
14. 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 Feb 20; 200():243-55. PubMed ID: 3001775 [No Abstract] [Full Text] [Related]
15. [Prenatal diagnosis of congenital adrenal hyperplasia due to a 21-hydroxylase defect--determination of 17-hydroxyprogesterone in the amniotic fluid]. Dumić M, Plavsić V, Ille J, Brkljacić L, Drazanćić A, Suchanek E, Kaśtelan A. Lijec Vjesn; 1987 Feb 20; 109(2-3):65-7. PubMed ID: 3496509 [No Abstract] [Full Text] [Related]
16. Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Morel Y, Miller WL. Adv Hum Genet; 1991 Feb 20; 20():1-68. PubMed ID: 1801590 [No Abstract] [Full Text] [Related]