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Items: 1 to 20 of 322

1.

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
2.

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.

[Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase enzyme deficiency].

Dumić M, Ille J, Brkljacić L, Plavsić V, Drazancić A, Banicević M, Radmanović S, Filipović B, Suchanek E, Kastelan A.

Lijec Vjesn. 1989 Sep-Oct;111(9-10):312-7. Croatian.

PMID:
2633007
6.

Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) in Croatia.

Dumic M, Brkljacic L, Plavsic V, Zunec R, Ille J, Wilson RC, Kuvacic I, Kastelan A, New MI.

Am J Med Genet. 1997 Oct 31;72(3):302-6.

PMID:
9332659
7.
8.
9.

'Cryptic' form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in the Yugoslav population.

Dumić M, Brkljacić L, Mardesić D, Plavsić V, Lukenda M, Kastelan A.

Acta Endocrinol (Copenh). 1985 Jul;109(3):386-92.

PMID:
2992207
10.

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
11.
12.

Prenatal diagnosis of congenital adrenal hyperplasia.

Warsof SL, Larsen JW, Kent SG, Rosenbaum KN, August GP, Migeon CJ, Schulman JD.

Obstet Gynecol. 1980 Jun;55(6):751-4.

PMID:
7383464
13.

Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.

Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI.

J Clin Endocrinol Metab. 1981 Dec;53(6):1193-8.

PMID:
6271801
15.

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
17.

Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency.

Speiser PW, New MI.

J Clin Endocrinol Metab. 1987 Jan;64(1):86-91.

PMID:
3023431
18.
19.

Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Lee PA, Rosenwaks Z, Urban MD, Migeon CJ, Bias WD.

J Clin Endocrinol Metab. 1982 Nov;55(5):866-71.

PMID:
6288754
20.

Prenatal diagnosis of congenital adrenal hyperplasia (21-OH deficiency type) by HLA typing.

Couillin P, Boue J, Nicolas H, Cheruy C, Boue A.

Prenat Diagn. 1981 Jan;1(1):25-33.

PMID:
6955777

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