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Items: 1 to 20 of 137

1.

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.

Mornet E, Boue J, Raux-Demay M, Couillin P, Oury JF, Dumez Y, Dausset J, Cohen D, Boué A.

Hum Genet. 1986 Aug;73(4):358-64.

PMID:
3017844
2.
3.

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;9(7):457-66.

PMID:
2788885
4.

HLA-A,B,C,DR typing and 17-OHP determination for second trimester prenatal diagnosis of 21-hydroxylase deficient CAH.

Grosse-Wilde H, Valentine-Thon E, Vögeler U, Passarge E, Lorenzen F, Sippell WG, Bidlingmaier F, Knorr D.

Prenat Diagn. 1988 Feb;8(2):131-43.

PMID:
3258985
5.

[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. Review. French. No abstract available.

PMID:
3006204
6.

Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluid.

Gueux B, Fiet J, Couillin P, Raux-Demay MC, Mornet E, Galons H, Villette JM, Boue J, Dreux C.

J Clin Endocrinol Metab. 1988 Mar;66(3):534-7.

PMID:
3258316
7.
8.

Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.

Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI.

Ann N Y Acad Sci. 1985;458:111-29. No abstract available.

PMID:
3879117
10.

Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.

Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI.

J Clin Endocrinol Metab. 1985 Jul;61(1):89-97.

PMID:
3873469
11.

[Genetic of the 21 hydroxylase deficiency].

Boué A, Couillin P, Pomarède R, Rappaport R, Boué J.

Ann Endocrinol (Paris). 1982;43(1):3-14. French.

PMID:
6982657
12.

Prenatal diagnosis of 21-hydroxylase deficiency by the complementary deoxyribonucleic acid probe for cytochrome P-450C-21OH.

Reindollar RH, Lewis JB, White PC, Fernhoff PM, McDonough PG, Whitney JB 3rd.

Am J Obstet Gynecol. 1988 Mar;158(3 Pt 1):545-7. Erratum in: Am J Obstet Gynecol 1988 Jun;158(6 Pt 1):1445.

PMID:
2831719
13.
14.

First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency).

Speiser PW, Laforgia N, Kato K, Pareira J, Khan R, Yang SY, Whorwood C, White PC, Elias S, Schriock E, et al.

J Clin Endocrinol Metab. 1990 Apr;70(4):838-48. Review.

PMID:
1969421
15.

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. No abstract available.

PMID:
3001775
16.
18.

Basic and clinical aspects of congenital adrenal hyperplasia.

New MI.

J Steroid Biochem. 1987;27(1-3):1-7. Review.

PMID:
3320531
19.

Prenatal DNA analysis in four embryos/fetuses at risk of 21-hydroxylase deficiency.

Matsumoto T, Kondoh T, Kamei T, Yoshimoto M, Tsuji Y, Suzumori K, Izumi R, Iwatani N, Niikawa N.

Eur J Pediatr. 1988 Dec;148(3):228-32.

PMID:
2905656
20.

[Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype].

Dzenis IG, Brykova EK, Bakharev VA.

Akush Ginekol (Mosk). 1990 Jan;(1):10-4. Russian. No abstract available.

PMID:
2353725

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