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Items: 1 to 20 of 119

1.

HLA-A, B, C, DR alleles in congenital adrenal hyperplasia.

Couillin P, Kottler-Missonnier ML, Grisard MC, Hors J, Feingold J, Boué J, Boué A.

Hum Genet. 1980;53(3):389-92.

PMID:
6966250
2.

HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency.

Pollack MS, New MI, O'Neill GJ, Levine LS, Callaway C, Pang S, 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, Dupont B.

Hum Genet. 1981;58(3):331-7.

PMID:
6948766
3.

Genetic linkage and HLA association in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Sobel DO, Gutai JP, Wagener DK, Jones JC, Smith WI, Strong DM.

Hum Immunol. 1983 May;7(1):35-44.

PMID:
6602118
4.

Linkage and association between HLA and 21-hydroxylase deficiency.

Klouda PT, Harris R, Price DA.

J Med Genet. 1980 Oct;17(5):337-41.

5.

21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.

Sinnott PJ, Dyer PA, Price DA, Harris R, Strachan T.

J Med Genet. 1989 Jan;26(1):10-7.

6.

HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France.

Couillin P, Rappaport R, Kuttenn F, Hors J, Feingold J, Boué J, Boué A.

Ann N Y Acad Sci. 1985;458:41-5. No abstract available.

PMID:
3879129
7.

Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients.

Fleischnick E, Awdeh ZL, Raum D, Granados J, Alosco SM, Crigler JF Jr, Gerald PS, Giles CM, Yunis EJ, Alper CA.

Lancet. 1983 Jan 22;1(8317):152-6.

PMID:
6130199
8.

Congenital adrenal hyperplasia--a clinical and genetic survey. Are we detecting male salt-losers?

Murtaza L, Sibert JR, Hughes I, Balfour IC.

Arch Dis Child. 1980 Aug;55(8):622-5.

9.

HLA and congenital adrenal hyperplasia.

Lisá L, Ivasková R, Sajdlová H, Kupková L.

Acta Paediatr Acad Sci Hung. 1981;22(4):267-74.

PMID:
7342672
10.

Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families.

Larizza D, Cuccia M, Martinetti M, Maghnie M, Dondi E, Salvaneschi L, Severi F.

Clin Endocrinol (Oxf). 1994 Jan;40(1):39-45.

PMID:
8306479
11.

Particular interest of HLA typing for genetic counselling in families with congenital adrenal hyperplasia (21-OH deficiency).

Couillin P, Boué J, Bétuel H, Hors J, Gebuhrer L, Boué A.

Haematologia (Budap). 1987;20(1):25-30.

PMID:
3496258
12.

Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.

Laron Z, Pollack MS, Zamir R, Roitman A, Dickerman Z, Levine LS, Lorenzen F, O'Neill GJ, Pang S, New MI, Dupont B.

Hum Immunol. 1980 Jul;1(1):55-66. No abstract available.

PMID:
6266983
13.

The coexistence of IgA deficiency and 21-hydroxylase deficiency marked by specific MHC supratypes.

Cobain TJ, Stuckey MS, McCluskey J, Wilton AN, Gedeon A, Garlepp MJ, Christiansen FT, Dawkins RL.

Ann N Y Acad Sci. 1985;458:76-84. No abstract available.

PMID:
3879134
14.

HLA-B14 and nonclassical 21-hydroxylase deficiency in a heterogeneous New York population.

Levine LS.

Ann N Y Acad Sci. 1985;458:65-70. No abstract available.

PMID:
3879132
16.

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.

PMID:
3493216
17.
18.

The HLA associations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a Yugoslav population.

Kastelan A, Brkljacić-Surkalović L, Dumić M.

Ann N Y Acad Sci. 1985;458:36-40. No abstract available.

PMID:
3879128
19.

HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.

Stuckey MS, Boyne P, Macdonald WB, Christiansen FT, Houliston JB, Dawkins RL.

Aust N Z J Med. 1980 Oct;10(5):552-4.

PMID:
6258552
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