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Similar articles for PubMed (Select 86832)

1.

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

Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon M, Owens RP, Merkatz IR, Nitowsky BM, Sachs G, Dupont B.

Lancet. 1979 May 26;1(8126):1107-8.

PMID:
86832
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
3.

HLA typing of amniotic-fluid cells applied to prenatal diagnosis of congenital adrenal hyperplasia.

Couillin P, Nicolas H, Boué J, Boué A.

Lancet. 1979 May 19;1(8125):1076. No abstract available.

PMID:
86789
4.

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
5.
6.

HLA and congenital adrenal hyperplasia linkage confirmed.

[No authors listed]

Lancet. 1978 Apr 29;1(8070):930-2. No abstract available.

PMID:
76861
7.

Technical and theoretical considerations in the HLA typing of amniotic fluid cells for prenatal diagnosis and paternity testing.

Pollack MS, Heagney SD, Braun D Jr, O'Neill GJ.

Prenat Diagn. 1981 Jul;1(3):183-95.

PMID:
6981107
8.

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

Milunsky A, Tulchinsky D.

Pediatrics. 1977 May;59(5):768-70. No abstract available.

PMID:
558577
9.

Prenatal diagnosis of congenital adrenal hyperplasia.

Marcus ES, Holcombe JH, Tulchinsky D, Rich RR, Riccardi VM.

Am J Med Genet. 1979;4(2):201-4.

PMID:
517576
10.

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).

Dupont B, Oberfield SE, Smithwick EM, Lee TD, Levine LS.

Lancet. 1977 Dec 24-31;2(8052-8053):1309-12.

PMID:
74726
12.

HLA typing of amniotic cells: the prenatal diagnosis of congenital adrenal hyperplasia (21-OH-deficiency type).

Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon MA, Owens RP, Merkatz IR, Nitowsky HM, Sachs G, Dupont B.

Transplant Proc. 1979 Dec;11(4):1726-8. No abstract available.

PMID:
394430
13.

[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
14.
15.

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
16.
17.

[Prenatal detection of congenital adrenal hyperplasia using HLA typing of fetal cells from the amniotic fluid].

Brkljacić L, Dumić M, Plavsić V, Drazancić A, Gerencer M, Kastelan A.

Lijec Vjesn. 1986 Nov-Dec;108(11-12):497-500. Croatian. No abstract available.

PMID:
3573974
18.

HLA typing of cultured amniotic cells for the prenatal diagnosis of complement C4 deficiency.

Pollack MS, Ochs HD, Dupont B.

Clin Genet. 1980 Sep;18(3):197-200. No abstract available.

PMID:
7438500
19.

Antenatal diagnosis of congenital adrenal hyperplasia.

Hughes IA, Laurence KM.

Lancet. 1979 Jul 7;2(8132):7-9.

PMID:
87946
20.
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