These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

91 related articles for article (PubMed ID: 9207613)

  • 1. Detection of CAH heterozygotes.
    Azziz R
    Fertil Steril; 1997 Jul; 68(1):183; discusssion 183-4. PubMed ID: 9207613
    [No Abstract]   [Full Text] [Related]  

  • 2. Detection of CAH heterozygotes.
    Chryssikopoulos A
    Fertil Steril; 1997 Jul; 68(1):182; author reply 183-4. PubMed ID: 9207612
    [No Abstract]   [Full Text] [Related]  

  • 3. Prenatal diagnosis of a heterozygote of salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency by genetic linkage analysis.
    Oh BH; Park JK; Choi YM; Yang IM; Kim YS; Choi YK
    J Korean Med Sci; 1988 Jun; 3(2):73-7. PubMed ID: 3267357
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detected heterozygotes during the molecular analysis of the common CYP21A2 point mutations in Macedonian patients with congenital adrenal hyperplasia and their relatives.
    Anastasovska V; Kocova M
    Prilozi; 2010; 31(2):71-82. PubMed ID: 21258279
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. [Genetic counseling in congenital adrenogenital syndrome].
    Blaim A; Ignaciuk A; Oblacińska A
    Pediatr Pol; 1982 Dec; 57(12):1107-11. PubMed ID: 7182790
    [No Abstract]   [Full Text] [Related]  

  • 7. Congenital adrenal hyperplasia.
    Loke KY
    J Singapore Paediatr Soc; 1991; 33(3-4):117-25. PubMed ID: 1812327
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Health status of adults with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Bachelot A; Touraine P
    Presse Med; 2014 Apr; 43(4 Pt 1):428-37. PubMed ID: 24630263
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case with combined rare inborn metabolic disorders: congenital adrenal hyperplasia and ornithine transcarbamylase deficiency.
    Kim YM; Lee BH; Choi JH; Kim GH; Lim HH; Yoo HW
    Gene; 2013 Sep; 527(1):394-6. PubMed ID: 23769969
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Detection of heterozygotes in the classic type of congenital adrenal hyperplasia due to a 21-hydroxylase defect in our population as based on hormonal studies and HLA typing].
    Dumić M; Tajić M; Brkljacić L; Mardesić D; Radica A; Lukenda M; Gjurić G; Jovanović V; Plavsić V; Kastelan A
    Lijec Vjesn; 1984; 106(11-12):466-70. PubMed ID: 6335215
    [No 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. [Congenital adrenogenital syndrome].
    Knorr D; Schwarz HP; Müller OA
    Internist (Berl); 1994 Mar; 35(3):219-25. PubMed ID: 8175285
    [No Abstract]   [Full Text] [Related]  

  • 13. 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. PubMed ID: 3873469
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S; Levine LS; Lorenzen F; Chow D; Pollack M; Dupont B; Genel M; New MI
    J Clin Endocrinol Metab; 1980 Mar; 50(3):586-9. PubMed ID: 6244328
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Late onset congenital adrenal hyperplasia in a Puerto Rican family: hormonal and HLA typing.
    Hernán Martínez J; Riestra JL
    Bol Asoc Med P R; 1986 Nov; 78(11):472-6. PubMed ID: 3026413
    [No Abstract]   [Full Text] [Related]  

  • 16. [Detection of heterozygosity in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the general population].
    Dumić M; Lukenda M; Plavsić V; Brkljacić L; Jovanović V; Kastelan A
    Lijec Vjesn; 1990; 112(5-6):138-41. PubMed ID: 2172673
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Potential advantage of N363S glucocorticoid receptor polymorphism in 21-hydroxylase deficiency.
    Luczay A; Török D; Ferenczi A; Majnik J; Sólyom J; Fekete G
    Eur J Endocrinol; 2006 Jun; 154(6):859-64. PubMed ID: 16728546
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene.
    Lekarev O; Tafuri K; Lane AH; Zhu G; Nakamoto JM; Buller-Burckle AM; Wilson TA; New MI
    J Perinatol; 2013 Jan; 33(1):76-8. PubMed ID: 23269230
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Molecular biology of the adrenogenital syndrome. New possibilities of heterozygote screening].
    Böhm BO; Rosak C; Böhm TL; White PC; Schöffling K
    Dtsch Med Wochenschr; 1987 Jan; 112(3):87-9. PubMed ID: 3492354
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Study of the transmission of the 21-hydroxylase deficiency through the hormonal screening and the HLA-typing (author's transl)].
    Bartolotta E; Migliori C; Gabrielli A; Oggiano N; Catassi C; Leone L
    Pediatr Med Chir; 1981; 3(4):287-90. PubMed ID: 6283486
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.