880 related articles for article (PubMed ID: 17932453)
1. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
Ogino W; Takeshima Y; Nishiyama A; Yagi M; Oka N; Matsuo M
Kobe J Med Sci; 2007; 53(4):143-50. PubMed ID: 17932453
[TBL] [Abstract][Full Text] [Related]
2. Tetrasomy 9p mosaicism associated with a normal phenotype in two cases.
Papoulidis I; Kontodiou M; Tzimina M; Saitis I; Hamid AB; Klein E; Kosyakova N; Kordass U; Kunz J; Siomou E; Nicolaides P; Orru S; Thomaidis L; Liehr T; Petersen MB; Manolakos E
Cytogenet Genome Res; 2012; 136(4):237-41. PubMed ID: 22487875
[TBL] [Abstract][Full Text] [Related]
3. Mosaic status in lymphocytes of infertile men with or without Klinefelter syndrome.
Lenz P; Luetjens CM; Kamischke A; Kühnert B; Kennerknecht I; Nieschlag E
Hum Reprod; 2005 May; 20(5):1248-55. PubMed ID: 15665007
[TBL] [Abstract][Full Text] [Related]
4. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
[TBL] [Abstract][Full Text] [Related]
5. Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report.
Velissariou V; Christopoulou S; Karadimas C; Pihos I; Kanaka-Gantenbein C; Kapranos N; Kallipolitis G; Hatzaki A
Eur J Med Genet; 2006; 49(4):331-7. PubMed ID: 16829354
[TBL] [Abstract][Full Text] [Related]
6. New case of mosaic tetrasomy 9p with additional neurometabolic findings.
Eggermann T; Rossier E; Theurer-Mainka U; Backsch C; Klein-Vogler U; Enders H; Kaiser P
Am J Med Genet; 1998 Feb; 75(5):530-3. PubMed ID: 9489799
[TBL] [Abstract][Full Text] [Related]
7. Case report of mosaic partial tetrasomy 9 mimicking Klinefelter syndrome.
Peters J; Pehl C; Miller K; Sandlin CJ
Birth Defects Orig Artic Ser; 1982; 18(3B):287-93. PubMed ID: 7139111
[No Abstract] [Full Text] [Related]
8. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
Zaki MS; Kamel AA; El-Ruby M
Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
[TBL] [Abstract][Full Text] [Related]
9. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.
de Azevedo Moreira LM; Freitas LM; Gusmão FA; Riegel M
Birth Defects Res A Clin Mol Teratol; 2003 Dec; 67(12):985-8. PubMed ID: 14745919
[TBL] [Abstract][Full Text] [Related]
10. Tetrasomy 9p: tissue-limited idic(9p) in a child with mild manifestations and a normal CVS result. Report and review.
Grass FS; Parke JC; Kirkman HN; Christensen V; Roddey OF; Wade RV; Knutson C; Spence JE
Am J Med Genet; 1993 Nov; 47(6):812-6. PubMed ID: 7506483
[TBL] [Abstract][Full Text] [Related]
11. Tetrasomy 9p mosaicism associated with a normal phenotype.
McAuliffe F; Winsor EJ; Chitayat D
Fetal Diagn Ther; 2005; 20(3):219-22. PubMed ID: 15824502
[TBL] [Abstract][Full Text] [Related]
12. Tissue-specific mosaicism for tetrasomy 9p uncovered by array CGH.
Shehab MI; Mazen I; Bint S
Am J Med Genet A; 2011 Oct; 155A(10):2496-2500. PubMed ID: 21998854
[TBL] [Abstract][Full Text] [Related]
13. Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization, and literature review.
Chen CP; Wang LK; Chern SR; Wu PS; Chen YT; Kuo YL; Chen WL; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2014 Mar; 53(1):79-85. PubMed ID: 24767652
[TBL] [Abstract][Full Text] [Related]
14. Tetrasomy Y by structural rearrangement: clinical report.
DesGroseilliers M; Lemyre E; Dallaire L; Lemieux N
Am J Med Genet; 2002 Sep; 111(4):401-4. PubMed ID: 12210299
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Pallister-Killian syndrome: Multiband FISH of tetrasomy 12p.
Gerdes AM; Hansen LK; Brandrup F; Soegaard K; Christoffersen A; Rasmussen K
Pediatr Dermatol; 2006; 23(4):378-81. PubMed ID: 16918638
[TBL] [Abstract][Full Text] [Related]
17. Klinefelter's syndrome, mosaic 46,XX/46,XY/47,XXY/48,XXXY/48,XXYY: a case report.
Al-Awadi SA; Teebi AS; Krishna Murthy DS; Othman G; Sundareshan TS
Ann Genet; 1986; 29(2):119-21. PubMed ID: 3490207
[TBL] [Abstract][Full Text] [Related]
18. Klinefelter variant mosaic with a reciprocal translocation t(1;7).
Vasu V; Chandra N; Jayashankar M; Santhiya ST
Fertil Steril; 2008 Nov; 90(5):2017.e15-7. PubMed ID: 18304545
[TBL] [Abstract][Full Text] [Related]
19. Karyotype revealed 47, xxy chromosome (Klinefelter syndrome): a case report.
Jha CB; Dhungel S; Rai D
Nepal Med Coll J; 2007 Sep; 9(3):215-6. PubMed ID: 18092444
[TBL] [Abstract][Full Text] [Related]
20. Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review.
El Khattabi L; Jaillard S; Andrieux J; Pasquier L; Perrin L; Capri Y; Benmansour A; Toutain A; Marcorelles P; Vincent-Delorme C; Journel H; Henry C; De Barace C; Devisme L; Dubourg C; Demurger F; Lucas J; Belaud-Rotureau MA; Amiel J; Malan V; De Blois MC; De Pontual L; Lebbar A; Le Dû N; Germain DP; Pinard JM; Pipiras E; Tabet AC; Aboura A; Verloes A
Am J Med Genet A; 2015 Jun; 167(6):1252-61. PubMed ID: 25847481
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
