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 *

149 related articles for article (PubMed ID: 9030973)

  • 21. Two XX males in one family and additional observations bearing on the etiology of XX males.
    Chapelle AD; Schröder J; Murros J; Tallqvist G
    Clin Genet; 1977 Feb; 11(2):91-106. PubMed ID: 837567
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Sex-determining region Y (SRY) in a patient with 46,XX true hermaphroditism.
    Tanoue A; Nakamura T; Endo F; Nishiyama S; Sakiyama H; Matsuda I
    Jpn J Hum Genet; 1992 Dec; 37(4):311-20. PubMed ID: 1297452
    [TBL] [Abstract][Full Text] [Related]  

  • 23. XX sex reversal: molecular analysis of the SRY/ZFY regions.
    Reddy PP; Papenhausen PR; Suh YM; Riddick LM; Calvano CJ; Mandell J
    J Urol; 1997 Sep; 158(3 Pt 2):1305-7. PubMed ID: 9258201
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical and molecular analysis of XX sex reversed patients.
    Kolon TF; Ferrer FA; McKenna PH
    J Urol; 1998 Sep; 160(3 Pt 2):1169-72; discussion 1178. PubMed ID: 9719302
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Clinical and genetic study of a 46, XX man with occult mosaicism ].
    Maciá Bobes C; Alonso Troncoso I; Botas Cervero P; Castaño Fernández G; Fau Cubero C
    Arch Esp Urol; 2002 Oct; 55(8):952-4. PubMed ID: 12455288
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular analysis in true hermaphroditism: demonstration of low-level hidden mosaicism for Y-derived sequences in 46,XX cases.
    Queipo G; Zenteno JC; Peña R; Nieto K; Radillo A; Dorantes LM; Eraña L; Lieberman E; Söderlund D; Jiménez AL; Ramón G; Kofman-Alfaro S
    Hum Genet; 2002 Sep; 111(3):278-83. PubMed ID: 12215841
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene.
    Turner B; Fechner PY; Fuqua JS; Marcantonio SM; Perlman EJ; Vordermark JS; Berkovitz GD
    Am J Med Genet; 1995 Jul; 57(3):440-3. PubMed ID: 7677147
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Sex genetics].
    Vilain E; Elreavey KM; Richaud F; Fellous M
    Presse Med; 1992 May; 21(18):852-6. PubMed ID: 1535151
    [TBL] [Abstract][Full Text] [Related]  

  • 29. DNA analyses of XX and XX-hypospadiac males.
    Numabe H; Nagafuchi S; Nakahori Y; Tamura T; Kiuchi H; Namiki M; Kohda N; Fukushima Y; Fuse H; Kusano M
    Hum Genet; 1992 Nov; 90(3):211-4. PubMed ID: 1487232
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Familial XX chromosomal maleness does not arise from a Y chromosomal translocation.
    Ostrer H; Wright G; Clayton M; Skordis N; MacGillivray MH
    J Pediatr; 1989 Jun; 114(6):977-82. PubMed ID: 2723912
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Reifenstein's syndrome: hereditary familial hypogonadism with hypospadias and gynecomastia.
    Jones LW; Isaacs H; Edelbrock H; Donnell GN
    J Urol; 1970 Oct; 104(4):608-11. PubMed ID: 5476478
    [No Abstract]   [Full Text] [Related]  

  • 32. Extended pedigree with multiple cases of XX sex reversal in the absence of SRY and of a mutation at the SOX9 locus.
    Temel SG; Gulten T; Yakut T; Saglam H; Kilic N; Bausch E; Jin WJ; Leipoldt M; Scherer G
    Sex Dev; 2007; 1(1):24-34. PubMed ID: 18391513
    [TBL] [Abstract][Full Text] [Related]  

  • 33. PCR analysis and sequencing of the SRY sex determining gene in four patients with bilateral congenital anorchia.
    Lobaccaro JM; Medlej R; Berta P; Belon C; Galifer RB; Guthmann JP; Chevalier C; Czernichow P; Dumas R; Sultan C
    Clin Endocrinol (Oxf); 1993 Feb; 38(2):197-201. PubMed ID: 8435900
    [TBL] [Abstract][Full Text] [Related]  

  • 34. PCR and FISH analysis of a ring Y chromosome.
    Henegariu O; Kernek S; Keating MA; Palmer CG; Heerema NA
    Am J Med Genet; 1997 Mar; 69(2):171-6. PubMed ID: 9056556
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Normal female phenotype and ovarian development despite the ovarian expression of the sex-determining region of Y chromosome (SRY) in a 46,XX/69,XXY diploid/triploid mosaic child conceived after in vitro fertilization-intracytoplasmic sperm injection.
    Oktem O; Paduch DA; Xu K; Mielnik A; Oktay K
    J Clin Endocrinol Metab; 2007 Mar; 92(3):1008-14. PubMed ID: 17164312
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Two SRY-negative XX male brothers without genital ambiguity.
    Zenteno JC; López M; Vera C; Méndez JP; Kofman-Alfaro S
    Hum Genet; 1997 Oct; 100(5-6):606-10. PubMed ID: 9341880
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 46,XX male: clinical, hormonal/genetic findings.
    Castiñeyra G; Copelli S; Levalle O
    Arch Androl; 2002; 48(4):251-7. PubMed ID: 12137585
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Analysis of clinical features and related genes variation in five patients with 46, XX male syndrome].
    Qin XY; Dong WK; Wang W; Dong ZY; Xiao Y; Lu WL; Wang DF
    Zhonghua Er Ke Za Zhi; 2016 Nov; 54(11):840-843. PubMed ID: 27806792
    [No Abstract]   [Full Text] [Related]  

  • 39. Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA.
    Jiménez AL; Kofman-Alfaro S; Berumen J; Hernández E; Canto P; Méndez JP; Zenteno JC
    Am J Med Genet; 2000 Aug; 93(5):417-20. PubMed ID: 10951467
    [TBL] [Abstract][Full Text] [Related]  

  • 40. An SRY-negative XX male with Huriez syndrome.
    Vernole P; Terrinoni A; Didona B; De Laurenzi V; Rossi P; Melino G; Grimaldi P
    Clin Genet; 2000 Jan; 57(1):61-6. PubMed ID: 10733237
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.