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4. [Genetic counseling in the adrenogenital syndrome caused by 2I-hydroxylase deficiency]. Breuning MH; Maaswinkel-Mooy PD Ned Tijdschr Geneeskd; 1986 Aug; 130(35):1552-5. PubMed ID: 3489897 [No Abstract] [Full Text] [Related]
5. [Prenatal diagnosis and therapy of adrenogenital syndrome with 21-hydroxylase deficiency. Position of the Pediatric Endocrinology Study Group of the German Society of Pediatrics and the Section of Pediatric Endocrinology of the German Society of Endocrinology]. Dörr HG; Sippell WG; Willig RP Monatsschr Kinderheilkd; 1992 Sep; 140(9):661-3. PubMed ID: 1435819 [No Abstract] [Full Text] [Related]
6. HLA typing as a method of genetic counselling in congenital adrenal hyperplasia. Savage MO; Field H; Wolf E; Pembrey ME; Grant DB Arch Dis Child; 1982 Apr; 57(4):315-7. PubMed ID: 6979315 [TBL] [Abstract][Full Text] [Related]
7. [Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups]. Cruz-Marin F; Raffoux C; Gilgenkrantz S; Janot C; Streiff F; Pierson M J Genet Hum; 1981 Mar; 29(1):103-13. PubMed ID: 6977617 [No Abstract] [Full Text] [Related]
8. [Prenatal molecular genetic diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency]. Rodríguez A; Ezquieta B; Varela JM; Moreno M; Dulín E; Rodríguez Arnao MD Med Clin (Barc); 1997 Nov; 109(17):669-72. PubMed ID: 9488957 [TBL] [Abstract][Full Text] [Related]
9. [21-hydroxylase deficiency: a case in a newborn revealing a maternal forme tardive]. Simonin G; Palix C; Roulier R; Coignet J Ann Pediatr (Paris); 1986 May; 33(5):423-7. PubMed ID: 3729253 [No Abstract] [Full Text] [Related]
10. Prenatal diagnosis and treatment of congenital adrenal hyperplasia. Nimkarn S; New MI Pediatr Endocrinol Rev; 2006 Dec-2007 Jan; 4(2):99-105. PubMed ID: 17342026 [TBL] [Abstract][Full Text] [Related]
11. [Carrier detection, prenatal diagnosis and treatment in adrenogenital syndrome]. Illy KE; Oosterwijk JC; Christiaens GC; Wit JM Ned Tijdschr Geneeskd; 1992 Dec; 136(49):2411-4. PubMed ID: 1470241 [No Abstract] [Full Text] [Related]
12. Infant with classic congenital adrenal hyperplasia (CAH) born to a mother with classic CAH. Nebesio TD; Kreher NC; Hannon TS J Pediatr; 2004 Aug; 145(2):250-2. PubMed ID: 15289778 [TBL] [Abstract][Full Text] [Related]
13. [Problems posed by the association of hemophilia A and congenital adrenal hyperplasia caused by 21-hydroxylase deficiency]. Boutte P; Madar H; d'Ollone M; Ferracci JP; Bebin B; Lambert JC; Sebag F Pediatrie; 1986; 41(7):559-64. PubMed ID: 3493478 [TBL] [Abstract][Full Text] [Related]
14. [Congenital adrenal hyperplasia, helping parents find their their bearings]. Gautheret L Soins Pediatr Pueric; 2011; (259):27. PubMed ID: 21520574 [No Abstract] [Full Text] [Related]
15. [Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency - different HLA genotypes in 2 brothers]. Dumić M; Plavsić V; Brkljacić L; Sarnavka V; Mardesić D; Tajić M; Kastelan A Lijec Vjesn; 1983 Apr; 105(4):145-9. PubMed ID: 6602259 [No Abstract] [Full Text] [Related]
16. P450scc deficiency (congenital lipoid adrenal hyperplasia): first reported case in Thailand and literature review. Jaruratanasirikul S J Med Assoc Thai; 1996 Aug; 79(8):531-5. PubMed ID: 8855637 [TBL] [Abstract][Full Text] [Related]