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 *

327 related articles for article (PubMed ID: 16276109)

  • 1. Complex mosaicism in sex reversed SRY+ male twins.
    DesGroseilliers M; Fortin F; Lemyre E; Lemieux N
    Cytogenet Genome Res; 2006; 112(1-2):176-9. PubMed ID: 16276109
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Unique karyotype: mos 46,X,dic(X;Y)(p22.33;p11.32)/ 45,X/45,dic(X;Y)(p22.33;p11.32) in an Egyptian patient with Ovotesticular disorder of sexual development.
    Mazen IM; Kamel AK; Mohamed AM; Hussien HA; Essawi ML; Hassan HA; El-Ruby MO; Aref A; Mekkawy MK
    Sex Dev; 2013; 7(5):235-43. PubMed ID: 23689268
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissue.
    Domenice S; Nishi MY; Billerbeck AE; Carvalho FM; Frade EM; Latronico AC; Arnhold IJ; Mendonca BB
    Med Sci Monit; 2001; 7(2):238-41. PubMed ID: 11257728
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Unusual maternal uniparental isodisomic x chromosome mosaicism with asymmetric y chromosomal rearrangement.
    Lee BY; Kim SY; Park JY; Choi EY; Kim DJ; Kim JW; Ryu HM; Cho YH; Park SY; Seo JT
    Cytogenet Genome Res; 2014; 142(2):79-86. PubMed ID: 24434812
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SRY-negative 46,XX male with normal genitals, complete masculinization and infertility.
    Rajender S; Rajani V; Gupta NJ; Chakravarty B; Singh L; Thangaraj K
    Mol Hum Reprod; 2006 May; 12(5):341-6. PubMed ID: 16556678
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosomal variants in klinefelter syndrome.
    Frühmesser A; Kotzot D
    Sex Dev; 2011; 5(3):109-23. PubMed ID: 21540567
    [TBL] [Abstract][Full Text] [Related]  

  • 7. XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin.
    Maciel-Guerra AT; de Mello MP; Coeli FB; Ribeiro ML; Miranda ML; Marques-de-Faria AP; Baptista MT; Moraes SG; Guerra-Júnior G
    J Clin Endocrinol Metab; 2008 Feb; 93(2):339-43. PubMed ID: 18056774
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
    Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
    Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 46,XX males: a case series based on clinical and genetics evaluation.
    Mohammadpour Lashkari F; Totonchi M; Zamanian MR; Mansouri Z; Sadighi Gilani MA; Sabbaghian M; Mohseni Meybodi A
    Andrologia; 2017 Sep; 49(7):. PubMed ID: 27882599
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Female karyotype and male phenotype: XX men. Apropos of 2 cases].
    Teyssier M; Moreau N
    J Gynecol Obstet Biol Reprod (Paris); 1986; 15(6):751-6. PubMed ID: 3098823
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences.
    Boucekkine C; Toublanc JE; Abbas N; Chaabouni S; Ouahid S; Semrouni M; Jaubert F; Toublanc M; McElreavey K; Vilain E
    Clin Endocrinol (Oxf); 1994 Jun; 40(6):733-42. PubMed ID: 8033363
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
    Reshmi SC; Miller JL; Deplewski D; Close C; Henderson LJ; Littlejohn E; Schwartz S; Waggoner DJ
    Eur J Med Genet; 2011; 54(2):161-4. PubMed ID: 21078420
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypes.
    Torres L; López M; Méndez JP; Canto P; Cervantes A; Alfaro G; Pérez-Palacios G; Erickson RP; Kofman-Alfaro S
    Am J Med Genet; 1996 May; 63(2):348-55. PubMed ID: 8725784
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial Turner syndrome with an X;Y translocation mosaicism: implications for genetic counseling.
    Portnoï MF; Chantot-Bastaraud S; Christin-Maitre S; Carbonne B; Beaujard MP; Keren B; Lévy J; Dommergues M; Cabrol S; Hyon C; Siffroi JP
    Eur J Med Genet; 2012 Nov; 55(11):635-40. PubMed ID: 22809487
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sex reversal due to Xp disomy by t(X;Y)(p21;q11).
    Vasquez AI; Rivera H; Mayorquin A; Mejia-Baltodano G; Escalante A; Sanchez-Corona J
    Genet Couns; 1999; 10(3):301-4. PubMed ID: 10546103
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.
    Abbas N; McElreavey K; Leconiat M; Vilain E; Jaubert F; Berger R; Nihoul-Fekete C; Rappaport R; Fellous M
    C R Acad Sci III; 1993; 316(4):375-83. PubMed ID: 8402263
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of new susceptibility regions for X;Y translocations in patients with testicular disorder of sex development.
    Beaulieu Bergeron M; Lemyre E; Lemieux N
    Sex Dev; 2011; 5(1):1-6. PubMed ID: 21088380
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.