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 *

181 related articles for article (PubMed ID: 7438488)

  • 21. Primary vitreoretinal dysplasia resembling Norrie's disease in a female: association with X autosome chromosomal translocation.
    Ohba N; Yamashita T
    Br J Ophthalmol; 1986 Jan; 70(1):64-71. PubMed ID: 3947601
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalities.
    Jacobs PA; Matsuura JS; Mayer M; Newlands IM
    Clin Genet; 1978 Jan; 13(1):37-60. PubMed ID: 146575
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Ring X and other structural X chromosome abnormalities: X inactivation and phenotype.
    Leppig KA; Disteche CM
    Semin Reprod Med; 2001 Jun; 19(2):147-57. PubMed ID: 11480912
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q.
    Sills JA; Buckton KE; Raeburn JA
    J Med Genet; 1976 Dec; 13(6):507-10. PubMed ID: 1018309
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Balanced chromosome abnormalities with abnormal phenotype].
    Fryns JP
    J Genet Hum; 1988 Jan; 36(1-2):33-6. PubMed ID: 3379377
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A cytogenetic study of nonpolymalformed patients with mental retardation of clinically undefined etiology: application of a high resolution banding technique.
    Kikkawa K; Narahara K; Kimoto H
    Acta Med Okayama; 1989 Apr; 43(2):105-14. PubMed ID: 2728904
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 10p- syndrome associated with multiple chromosomal abnormalities.
    Prieto F; Badia L; Moreno JA; Barbero P; Asensi F
    Hum Genet; 1978 Dec; 45(2):229-35. PubMed ID: 738725
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 49, XXXXY karyotype in mentally retarded boy.
    Morić-Petrović S; Laca Z; Marković S; Marković V
    J Ment Defic Res; 1973 Mar; 17(1):73-80. PubMed ID: 4795155
    [No Abstract]   [Full Text] [Related]  

  • 29. Double balanced de novo translocations involving chromosomes 4/15 and 5/12 in a mentally retarded boy.
    Li SY; Jong RH; Chow MC; Jou TC
    Proc Natl Sci Counc Repub China B; 1984 Jan; 8(1):54-9. PubMed ID: 6531417
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Effect of balanced X/autosome translocations on sexual and physical development. A personal experience in 4 patients.
    Kleczkowska A; Fryns JP; Vinken L; van den Berghe H
    Clin Genet; 1985 Feb; 27(2):147-52. PubMed ID: 3978849
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Complex chromosome rearrangement involving chromosomes 1, 4 and 16 revealed by fluorescence in situ hybridization.
    Johannesson T; Ehlers S; Wahlström J
    Clin Genet; 1997 Apr; 51(4):281-5. PubMed ID: 9184255
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Alpha-thalassemia/mental retardation syndrome in a 45,X male.
    Kellermayer R; Czakó M; Kiss-László Z; Gyuris P; Kozári A; Melegh B; Kosztolányi G
    Am J Med Genet A; 2005 Feb; 132A(4):431-3. PubMed ID: 15633163
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report.
    Tsutsumi M; Hattori H; Akita N; Maeda N; Kubota T; Horibe K; Fujita N; Kawai M; Shinkai Y; Kato M; Kato T; Kawamura R; Suzuki F; Kurahashi H
    BMC Med Genomics; 2019 Dec; 12(1):182. PubMed ID: 31806026
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The origin of telocentric chromosomes in man: a girl with tel(Xq).
    Therman E; Sarto GE; DeMars RI
    Hum Genet; 1981; 57(1):104-7. PubMed ID: 7262864
    [TBL] [Abstract][Full Text] [Related]  

  • 35. X-linked mental retardation with a fragile site in Xq and an inversion of chromosome no. 9.
    Howard-Peebles PN
    Hum Hered; 1982; 32(2):139-41. PubMed ID: 7201453
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Inherited partial X chromosome duplication in a mentally retarded male.
    Nielsen KB; Langkjaer F
    J Med Genet; 1982 Jun; 19(3):222-4. PubMed ID: 7108918
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation.
    Chen CP; Lin SP; Chern SR; Kuo YL; Wu PS; Chen YT; Lee MS; Wang W
    Gene; 2014 Feb; 535(1):88-92. PubMed ID: 24279999
    [TBL] [Abstract][Full Text] [Related]  

  • 39. X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter.
    Madan K; Hompes PG; Schoemaker J; Ford CE
    Hum Genet; 1981; 59(4):290-6. PubMed ID: 7333583
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Characterisation, phenotypic manifestations and X-inactivation pattern in 14 patients with X-autosome translocations.
    Kalz-Füller B; Sleegers E; Schwanitz G; Schubert R
    Clin Genet; 1999 May; 55(5):362-6. PubMed ID: 10422808
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.