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 *

141 related articles for article (PubMed ID: 3211844)

  • 1. XX/XY chimerism encountered during prenatal diagnosis.
    Freiberg AS; Blumberg B; Lawce H; Mann J
    Prenat Diagn; 1988 Jul; 8(6):423-6. PubMed ID: 3211844
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 45,X/46,XY mosaicism: the role of ultrasound in prenatal diagnosis and counselling.
    Lazebnik N; Filkins KA; Jackson CL; Linn KB; Doshi NN; Hogge WA
    Ultrasound Obstet Gynecol; 1996 Nov; 8(5):325-8. PubMed ID: 8978006
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera.
    Chen CP; Chern SR; Sheu JC; Lin SP; Hsu CY; Chang TY; Lee CC; Wang W; Chen HE
    Prenat Diagn; 2005 Jun; 25(6):502-6. PubMed ID: 15966046
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diagnostic applications of H-Y serology: H-Y negative phenotype in cells from 45,X/46,XY fetus with testes.
    Lieber E; Wachtel SS; Aftalion B; Zaslav AL
    Clin Genet; 1986 Nov; 30(5):366-73. PubMed ID: 3802555
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia.
    Kawamura R; Kato T; Miyai S; Suzuki F; Naru Y; Kato M; Tanaka K; Nagasaka M; Tsutsumi M; Inagaki H; Ioroi T; Yoshida M; Nao T; Conlin LK; Iijima K; Kurahashi H; Taniguchi-Ikeda M
    J Hum Genet; 2020 Aug; 65(8):705-709. PubMed ID: 32277176
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 46,XX/46XY chromosome complement in amniotic fluid cell culture followed by the birth of a normal female child.
    Hunter A; Brierley K; Tomkins D
    Prenat Diagn; 1982 Apr; 2(2):127-31. PubMed ID: 7145839
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination.
    Cheng D; Lu CF; Gong F; Du J; Yuan S; Luo KL; Tan YQ; Lu GX; Lin G
    Hum Reprod; 2024 Apr; 39(4):849-855. PubMed ID: 38420683
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of 45,X/46,XX mosaicism and 45,X: implications for postnatal outcome.
    Koeberl DD; McGillivray B; Sybert VP
    Am J Hum Genet; 1995 Sep; 57(3):661-6. PubMed ID: 7668295
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two equine true hermaphrodites with 64,XX/64,XY and 63,XO/64,XY chimerism.
    Dunn HO; Smiley D; Duncan JR; McEntee K
    Cornell Vet; 1981 Apr; 71(2):123-35. PubMed ID: 7194168
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of tetrasomy 47,XY,+i(12p) confirmed by in situ hybridization.
    Shivashankar L; Whitney E; Colmorgen G; Young T; Munshi G; Wilmoth D; Byrne K; Reeves G; Borgaonkar DS; Picciano SR
    Prenat Diagn; 1988 Feb; 8(2):85-91. PubMed ID: 3362782
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of 45, X/46, XY.
    Waurin JL; Adams JE; Baramki TA
    Md Med J; 1985 Sep; 34(9):883-4. PubMed ID: 3851135
    [No Abstract]   [Full Text] [Related]  

  • 13. [Application of fluorescence insitu hybridization technique for prenatal diagnosis of chromosome abnormality in amniotic cells].
    Huang Y; Sun X; Li Q
    Zhonghua Fu Chan Ke Za Zhi; 1999 Mar; 34(3):153-5. PubMed ID: 11263185
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case report.
    Malan V; Gesny R; Morichon-Delvallez N; Aubry MC; Benachi A; Sanlaville D; Turleau C; Bonnefont JP; Fekete-Nihoul C; Vekemans M
    Hum Reprod; 2007 Apr; 22(4):1037-41. PubMed ID: 17272360
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatally diagnosed 45,X/46,XY and normal phenotype.
    Chang HJ; Clark RD; Bachman H
    Lancet; 1989 Apr; 1(8644):961-2. PubMed ID: 2565452
    [No Abstract]   [Full Text] [Related]  

  • 16. Origin of chi46,XX/46,XY chimerism in a human true hermaphrodite.
    Dewald G; Haymond MW; Spurbeck JL; Moore SB
    Science; 1980 Jan; 207(4428):321-3. PubMed ID: 7350665
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dispermic chimerism with two abnormal cell lines, 47,XY, +21 and 47,XX, +12.
    Wiley JE; Madigan M; Christie JD; Smith AW
    Am J Med Genet; 2002 Jan; 107(1):64-6. PubMed ID: 11807871
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Identification of Y chromosome material in an XX male by means of fluorescent in situ hybridization].
    Brandt CA; Hindkjaer J; Strømkjaer H; Christensen MF; Kølvraa S
    Ugeskr Laeger; 1992 Nov; 154(47):3321-4. PubMed ID: 1462437
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Urethral diverticulum in a calf with XX/XY chimerism.
    Strabel D; Schweizer G; Camenisch U; Stranzinger G; Braun U
    Vet Rec; 2003 May; 152(22):690-1. PubMed ID: 12803398
    [No Abstract]   [Full Text] [Related]  

  • 20. Use of probes for ZFY, SRY, and the Y pseudoautosomal boundary in XX males, XX true hermaphrodites, and an XY female.
    Pereira ET; de Almeida JC; Gunha AC; Patton M; Taylor R; Jeffery S
    J Med Genet; 1991 Sep; 28(9):591-5. PubMed ID: 1956056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.