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 *

204 related articles for article (PubMed ID: 475436)

  • 21. Ring chromosome 16: a new case.
    Vianello MG; Cottafava F; Bartoli D; Franzone G; Casazzava R; Gastaldi R
    Ann Genet; 1990; 33(1):36-9. PubMed ID: 2195979
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Chromosome instability limited to the aneuploid clone in the Pallister-Killian syndrome: a pitfall in prenatal diagnosis.
    Zollino M; Bajer J; Neri G
    Prenat Diagn; 1999 Feb; 19(2):184-5. PubMed ID: 10215084
    [No Abstract]   [Full Text] [Related]  

  • 23. Chromosomal rearrangements and mental retardation.
    Agostoni C
    Pediatr Res; 2000 Apr; 47(4 Pt 1):429. PubMed ID: 10759144
    [No Abstract]   [Full Text] [Related]  

  • 24. Pericentric inversion of chromosome 7 (inv(7) (p22q11.2)) and ring chromosome 8 (r(8) (p23q24.3)) in a girl with minor anomalies.
    Verma RS; Conte RA; Pitter JH; Luke S
    J Med Genet; 1992 Jan; 29(1):66-7. PubMed ID: 1552550
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Mental retardation and sexual development in chromosomal syndrome (author's transl)].
    Balestrazzi P; Bernasconi S; Medioli FC; Corrini L; Villani G
    Ateneo Parmense Acta Biomed; 1980; 51(1):45-51. PubMed ID: 7470180
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Outcome for patients with constitutional 13q chromosomal abnormalities and retinoblastoma.
    Pratt CB; Raimondi SC; Kaste SC; Heaton DM; Mounce KG; Mandrell B; Crom D; Meyer D
    Pediatr Hematol Oncol; 1994; 11(5):541-7. PubMed ID: 7826849
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Chromosome studies in patients with congenital malformations and mental retardation.
    Erdtmann B; Salzano FM; Mattevi MS
    Humangenetik; 1975; 26(4):297-306. PubMed ID: 1150230
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cytogenetic and clinical studies in five cases of inv dup(15).
    Wisniewski L; Hassold T; Heffelfinger J; Higgins JV
    Hum Genet; 1979 Sep; 50(3):259-70. PubMed ID: 489010
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two cases of ring chromosome 11.
    Romain DR; Gebbie OB; Parfitt RG; Columbano-Green LM; Smythe RH; Chapman CJ; Kerr A
    J Med Genet; 1983 Oct; 20(5):380-2. PubMed ID: 6315941
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Phenotypic variation in two patients with a ring chromosome 22.
    Funderburk SJ; Sparkes RS; Klisak I
    Clin Genet; 1979 Nov; 16(5):305-10. PubMed ID: 519902
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The cytogenetics of 90 patients with idiopathic mental retardation/malformation syndromes and of 90 normal subjects.
    Doyle CT
    Hum Genet; 1976 Jul; 33(2):131-46. PubMed ID: 939565
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cytogenetics of 50 patients with mental retardation and multiple congenital anomalies and 50 normal subjects. Madison blind study IV.
    Magnelli NC
    Clin Genet; 1976 Feb; 9(2):169-82. PubMed ID: 1248176
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Ring chromosome 4 in twins].
    Giuffrè L; Cammarata M; Corsello G; Benigno V; Graziano L; Roccella F; Balsamo V
    Pediatr Med Chir; 1987; 9(3):349-50. PubMed ID: 3671134
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Ring chromosome 5 associated with severe growth retardation as the sole major physical abnormality.
    Migliori MV; Cherubini V; Bartolotta E; Pettinari A; Pecora R
    Am J Med Genet; 1994 Jan; 49(1):108-10. PubMed ID: 8172236
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal recognition of 4p- syndrome.
    Blunt S; Berry AC; Seller MJ; Williams CA
    J Med Genet; 1977 Jun; 14(3):232-3. PubMed ID: 881719
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Clinical and genetic study of a child with mental retardation and multiple congenital anomalies and a 16p13.11 microdeletion].
    Wang H; Xiao B; Ye H; Hu Q; Qiu W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug; 33(4):485-9. PubMed ID: 27455003
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [De novo t(3 ; 20) (p 14 ; p 12) translocation in a young girl].
    Stoll C; Levy JM
    Ann Genet; 1974 Sep; 17(3):197-9. PubMed ID: 4548822
    [No Abstract]   [Full Text] [Related]  

  • 38. [A new clinico-cytogenetic syndrome--a proximal deletion of the short arm of chromosome 17].
    Zaletaev DV; Marincheva GS
    Pediatriia; 1988; (11):82-4. PubMed ID: 3226810
    [No Abstract]   [Full Text] [Related]  

  • 39. Two cases of an abnormal short arm of chromosome 8 (8p+) associated with mental retardation.
    Hongell K; Knuutila S; Westermarck T
    Clin Genet; 1978 Feb; 13(2):237-40. PubMed ID: 627113
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Duplication 14(q31----qter).
    Carr DM; Jones-Quartey K; Vartanian MV; Moore-Kaplan H
    J Med Genet; 1987 Jun; 24(6):372-4. PubMed ID: 3612709
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.