89 related articles for article (PubMed ID: 2773999)
21. FISH analysis for apparently simple terminal deletions of the X chromosome: identification of hidden structural abnormalities.
Ogata T; Matsuo N; Fukushima Y; Saito M; Nose O; Miharu N; Uehara S; Ishizuka B
Am J Med Genet; 2001 Dec; 104(4):307-11. PubMed ID: 11754066
[TBL] [Abstract][Full Text] [Related]
22. The behavior of sex chromosomes in two human X-autosome translocations: failure of extensive X-inactivation spreading.
Solari AJ; Rahn IM; Ferreyra ME; Carballo MA
Biocell; 2001 Aug; 25(2):155-66. PubMed ID: 11590891
[TBL] [Abstract][Full Text] [Related]
23. X chromosome inactivation and X-linked mental retardation.
Willard HF
Am J Med Genet; 1996 Jul; 64(1):21-6. PubMed ID: 8826443
[TBL] [Abstract][Full Text] [Related]
24. Trisomy Xq in a male: the isochromosome X Klinefelter syndrome.
Donlan MA; Dolan CR; Metcalf MJ; Bradley CM; Salk D
Am J Med Genet; 1987 May; 27(1):189-94. PubMed ID: 3605195
[TBL] [Abstract][Full Text] [Related]
25. Deletions of Xq and growth deficit: a review.
Geerkens C; Just W; Vogel W
Am J Med Genet; 1994 Apr; 50(2):105-13. PubMed ID: 8010343
[TBL] [Abstract][Full Text] [Related]
26. A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family.
Karaman B; Wollnik B; Ermiş H; Yüksel-Apak M; Başaran S
Prenat Diagn; 2003 Apr; 23(4):336-9. PubMed ID: 12673642
[TBL] [Abstract][Full Text] [Related]
27. Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome.
Kusz K; Kotecki M; Wojda A; Szarras-Czapnik M; Latos-Bielenska A; Warenik-Szymankiewicz A; Ruszczynska-Wolska A; Jaruzelska J
J Med Genet; 1999 Jun; 36(6):452-6. PubMed ID: 10874632
[TBL] [Abstract][Full Text] [Related]
28. A ring X chromosome, 46,Y,r(X)(p22.33q28), as a cause of extreme short stature in a male.
Ogata T; Matsuo N; Shimizu N
Am J Med Genet; 1990 Feb; 35(2):241-4. PubMed ID: 2106786
[TBL] [Abstract][Full Text] [Related]
29. Short stature in a mother and daughter with terminal deletion of Xp22.3.
Schwinger E; Kirschstein M; Greiwe M; Konermann T; Orth U; Gal A
Am J Med Genet; 1996 May; 63(1):239-42. PubMed ID: 8723116
[TBL] [Abstract][Full Text] [Related]
30. Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma.
Kajii T; Tsukahara M; Fukushima Y; Hata A; Matsuo K; Kuroki Y
Ann Genet; 1985; 28(4):219-23. PubMed ID: 3879432
[TBL] [Abstract][Full Text] [Related]
31. [A case of X/X translocation: t(X;X) (q26;p11)].
Wagenbichler P; Frisch H; Schnedl W
Klin Padiatr; 1975 Nov; 187(6):533-7. PubMed ID: 765610
[TBL] [Abstract][Full Text] [Related]
32. A recombinant X chromosome in a short statured girl resulting from a maternal pericentric inversion.
Duckett DP; Young ID
Hum Genet; 1988 Jul; 79(3):251-4. PubMed ID: 3042599
[TBL] [Abstract][Full Text] [Related]
33. Sex chromosomal abnormalities. Etiology, phenotypic expression, and the role of lyonization.
Ho HZ
ASHA; 1990 Sep; 32(9):48-50. PubMed ID: 2222563
[TBL] [Abstract][Full Text] [Related]
34. Partial Xp duplication in a girl with dysmorphic features: the change in replication pattern of late-replicating dupX chromosome.
Kokalj Vokac N; Seme Ciglenecki P; Erjavec A; Zagradisnik B; Zagorac A
Clin Genet; 2002 Jan; 61(1):54-61. PubMed ID: 11903357
[TBL] [Abstract][Full Text] [Related]
35. Random X inactivation in a girl with a balanced t(X;9) and an abnormal phenotype.
Wolff DJ; Schwartz S; Montgomery T; Zackowski JL
Am J Med Genet; 1998 Jun; 77(5):401-4. PubMed ID: 9632170
[TBL] [Abstract][Full Text] [Related]
36. A new syndrome with mental retardation, short stature and an Xq duplication.
Thode A; Partington MW; Yip MY; Chapman C; Richardson VF; Turner G
Am J Med Genet; 1988; 30(1-2):239-50. PubMed ID: 3177451
[TBL] [Abstract][Full Text] [Related]
37. A familial Xp+ chromosome, dup (Xq26.3-->qter).
Vasquez AI; Rivera H; Bobadilla L; Crolla JA
J Med Genet; 1995 Nov; 32(11):891-3. PubMed ID: 8592335
[TBL] [Abstract][Full Text] [Related]
38. Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother.
Panasiuk B; Midro AT; Zadrozna-Tołwińska B
Clin Genet; 1997 Aug; 52(2):120-5. PubMed ID: 9298748
[TBL] [Abstract][Full Text] [Related]
39. Karyotype/phenotype correlation in females with short stature.
Temtamy SA; Ghali I; Salam MA; Hussein FH; Ezz EH; Salah N
Clin Genet; 1992 Mar; 41(3):147-51. PubMed ID: 1563089
[TBL] [Abstract][Full Text] [Related]
40. Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy.
Ottesen AM; Aksglaede L; Garn I; Tartaglia N; Tassone F; Gravholt CH; Bojesen A; Sørensen K; Jørgensen N; Rajpert-De Meyts E; Gerdes T; Lind AM; Kjaergaard S; Juul A
Am J Med Genet A; 2010 May; 152A(5):1206-12. PubMed ID: 20425825
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]