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25. Lack of X inactivation: loss of one X inactivation center in a case with mos45,X,-21, +der(21)t(X;21) (p21.3;p11.2)/46,X,t(X;21) (p21.3;p11.2). Ishikiriyama S; Iai M; Tanabe Y Am J Med Genet; 1993 Aug; 47(1):41-4. PubMed ID: 8368250 [TBL] [Abstract][Full Text] [Related]
26. Marker X syndrome in an oriental family with probable transmission by a normal male. Rhoads FA; Oglesby AC; Mayer M; Jacobs PA Am J Med Genet; 1982 Jun; 12(2):205-17. PubMed ID: 7102725 [TBL] [Abstract][Full Text] [Related]
27. Brief clinical report: renal hypodysplasia and unilateral ovarian agenesis in the penta-X syndrome. Toussi T; Halal F; Lesage R; Delorme F; Bergeron A Am J Med Genet; 1980; 6(2):153-62. PubMed ID: 7446561 [TBL] [Abstract][Full Text] [Related]
30. De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype. Tihy F; Lemyre E; Lemieux N; Dallaire L Am J Med Genet; 1999 Dec; 87(4):302-5. PubMed ID: 10588834 [TBL] [Abstract][Full Text] [Related]
31. Escalante syndrome and the marker X chromosome. Vianna-Morgante AM; Armando I; Frota-Pessoa O Am J Med Genet; 1982 Jun; 12(2):237-40. PubMed ID: 7201744 [No Abstract] [Full Text] [Related]
32. Mental retardation, megalotestes and a marker X chromosome. Fitzsimmons J; McLachlan JI; Fitzsimmons E; Cooke P Practitioner; 1982 Apr; 226(1366):735-41. PubMed ID: 6953399 [No Abstract] [Full Text] [Related]
34. The fragile X chromosome mental retardation and large testes. Hecht F; Kaiser-McCaw B; Moore BC; Cadien J; Glover TW Ariz Med; 1980 Nov; 37(11):764-6. PubMed ID: 7224864 [No Abstract] [Full Text] [Related]
35. [Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication]. Reichenbach H; Holland H; Thamm B; Theile T Kinderarztl Prax; 1993 Oct; 61(7-8):291-5. PubMed ID: 8271681 [TBL] [Abstract][Full Text] [Related]
36. Aicardi syndrome: a variant example with new clinical findings. Gedik Y; Erduran E; Aslan Y; Soyluf H; Mocan H; Demirci A Genet Couns; 1993; 4(4):281-3. PubMed ID: 8110415 [TBL] [Abstract][Full Text] [Related]
37. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation. Brooks SS; Wisniewski K; Brown WT Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044 [TBL] [Abstract][Full Text] [Related]
38. Triple-X syndrome accompanied by single maxillary central incisor: case report. Miura M; Kato N; Kojima H; Oguchi H Pediatr Dent; 1993; 15(3):214-7. PubMed ID: 8378162 [TBL] [Abstract][Full Text] [Related]
39. Tall stature, gonadal dysgenesis, and stigmata of Turner's syndrome caused by a structurally altered X chromosome. Binder G; Eggermann T; Enders H; Ranke MB; Dufke A J Pediatr; 2001 Feb; 138(2):285-7. PubMed ID: 11174634 [TBL] [Abstract][Full Text] [Related]
40. Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome). Jennings M; Hall JG; Hoehn H Am J Med Genet; 1980; 7(4):417-32. PubMed ID: 6938131 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]