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 *

207 related articles for article (PubMed ID: 6536471)

  • 21. [Congenital genital anomalies. Aspects of diagnostics and treatment].
    Zaparackaite I; Barauskas V
    Medicina (Kaunas); 2003; 39(2):105-13. PubMed ID: 12626862
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients.
    Maimoun L; Philibert P; Cammas B; Audran F; Bouchard P; Fenichel P; Cartigny M; Pienkowski C; Polak M; Skordis N; Mazen I; Ocal G; Berberoglu M; Reynaud R; Baumann C; Cabrol S; Simon D; Kayemba-Kay's K; De Kerdanet M; Kurtz F; Leheup B; Heinrichs C; Tenoutasse S; Van Vliet G; Grüters A; Eunice M; Ammini AC; Hafez M; Hochberg Z; Einaudi S; Al Mawlawi H; Nuñez CJ; Servant N; Lumbroso S; Paris F; Sultan C
    J Clin Endocrinol Metab; 2011 Feb; 96(2):296-307. PubMed ID: 21147889
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Testicular feminization. Cases of the Iaşi Endocrinology Clinic].
    Tiron V; Pencea V; Covic M; Pricop M
    Rev Med Chir Soc Med Nat Iasi; 1985; 89(1):89-92. PubMed ID: 4070882
    [No Abstract]   [Full Text] [Related]  

  • 24. [Sex differentiation disorders: male pseudohermaphroditism. Clinical and etiopathogenetic forms and behavioral aspects].
    Zbranca E; Mogoş V
    Rev Med Chir Soc Med Nat Iasi; 1986; Suppl():295-303. PubMed ID: 3317669
    [No Abstract]   [Full Text] [Related]  

  • 25. Female phenotype associated with XY karyotype: report of a case with gonadal dysgenesis.
    Smith M; Pepler WJ
    S Afr Med J; 1969 Nov; 43(46):1414-5. PubMed ID: 5361329
    [No Abstract]   [Full Text] [Related]  

  • 26. [External male pseudoherm (diagnosis and classification)].
    Pawlikoswki T; Reterski Z
    Endokrynol Pol; 1968; 19(5):513-8. PubMed ID: 5708765
    [No Abstract]   [Full Text] [Related]  

  • 27. Androgen insensitivity syndrome in a cohort of Sri Lankan children with 46, XY disorders of sex development (46, XY DSD).
    de Silva KS; Sirisena ND; Wijenayaka HK; Cooray JG; Jayasekara RW; Dissanayake VH
    Ceylon Med J; 2015 Dec; 60(4):139-42. PubMed ID: 26778393
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Female phenotype in a male child due to 17-alpha-hydroxylase deficiency.
    Heremans GF; Moolenaar AJ; van Gelderen HH
    Arch Dis Child; 1976 Sep; 51(9):721-3. PubMed ID: 999330
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Male pseudohermaphroditism.
    Kupfer SR; Quigley CA; French FS
    Semin Perinatol; 1992 Oct; 16(5):319-31. PubMed ID: 1485188
    [No Abstract]   [Full Text] [Related]  

  • 30. Familial occurrence of male pseudohermaphrodites with ambiguous external genitals.
    Boczkowski K; Wawryk R; Krupa B; Mickiewicz E
    Am J Obstet Gynecol; 1972 Jan; 112(2):192-8. PubMed ID: 5008446
    [No Abstract]   [Full Text] [Related]  

  • 31. Clinical and molecular aspects of androgen insensitivity.
    Hiort O
    Endocr Dev; 2013; 24():33-40. PubMed ID: 23392093
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The infant with ambiguous genitalia.
    Moloshok RE; Kerr JM
    Pediatr Clin North Am; 1972 Aug; 19(3):529-42. PubMed ID: 5039348
    [No Abstract]   [Full Text] [Related]  

  • 33. Sex redefined.
    Ainsworth C
    Nature; 2015 Feb; 518(7539):288-91. PubMed ID: 25693544
    [No Abstract]   [Full Text] [Related]  

  • 34. [Differential diagnosis and treatment of girls with 46XY-karyotype and androgen insensitivity syndrome].
    Drop SL; Boehmer AL; Slijper FM; Nijman JM; Hazebroek FW; Niermeijer MF
    Ned Tijdschr Geneeskd; 2001 Apr; 145(14):665-9. PubMed ID: 11530701
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Clinical and genetical studies in testicular feminization syndrome].
    Boczkowski K
    Ginekol Pol; 1969 May; 40(5):549-57. PubMed ID: 5805689
    [No Abstract]   [Full Text] [Related]  

  • 36. AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity.
    Akcay T; Fernandez-Cancio M; Turan S; Güran T; Audi L; Bereket A
    Andrology; 2014 Jul; 2(4):572-8. PubMed ID: 24737579
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Male patients with partial androgen insensitivity syndrome: a longitudinal follow-up of growth, reproductive hormones and the development of gynaecomastia.
    Hellmann P; Christiansen P; Johannsen TH; Main KM; Duno M; Juul A
    Arch Dis Child; 2012 May; 97(5):403-9. PubMed ID: 22412043
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genotype versus phenotype in families with androgen insensitivity syndrome.
    Boehmer AL; Brinkmann O; Brüggenwirth H; van Assendelft C; Otten BJ; Verleun-Mooijman MC; Niermeijer MF; Brunner HG; Rouwé CW; Waelkens JJ; Oostdijk W; Kleijer WJ; van der Kwast TH; de Vroede MA; Drop SL
    J Clin Endocrinol Metab; 2001 Sep; 86(9):4151-60. PubMed ID: 11549642
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Intersexual forms in children and social-pediatric problems].
    Glatzl J
    Wien Med Wochenschr; 1970 Jun; 120(23):413-7. PubMed ID: 5520883
    [No Abstract]   [Full Text] [Related]  

  • 40. The XY female child.
    Dewhurst CJ
    Arch Dis Child; 1970 Aug; 45(242):595-9. PubMed ID: 5528744
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.