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 *

1043 related articles for article (PubMed ID: 6235655)

  • 41. [Pericentric inversion of a chromosome 21. Study of 3 generations. Genetic counseling].
    Fraisse J
    J Genet Hum; 1975 Oct; 23 SUPPL():107-11. PubMed ID: 129537
    [No Abstract]   [Full Text] [Related]  

  • 42. Probable reciprocal translocation in somatic cells from patients with Down's syndrome.
    Sonta S; Oishi H
    Jinrui Idengaku Zasshi; 1974 Sep; 19(2):169-73. PubMed ID: 4280457
    [No Abstract]   [Full Text] [Related]  

  • 43. [Significance of chromosome translocations from the G-D group in the karyotype of the mother of 2 children with Down's syndrome].
    Dobrzańska A; Kostrzewski J
    Pediatr Pol; 1970 Feb; 45(2):211-5. PubMed ID: 4245096
    [No Abstract]   [Full Text] [Related]  

  • 44. Pericentric inversion of chromosome 13: familial study and review of the literature.
    Fernández-Novoa C; Vargas T; Fernández-Ortega JM; Gonzalez V; Duenas J
    Genet Couns; 1991; 2(3):133-8. PubMed ID: 1839355
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Inv21p12q22del21q22 and intellectual disability.
    Oliveira R; Dória S; Madureira C; Lima V; Almeida C; Pinho MJ; Ramalho C; Matoso E; Barros A; Carreira IM; Moura CP
    Gene; 2013 Mar; 517(1):120-4. PubMed ID: 23266646
    [TBL] [Abstract][Full Text] [Related]  

  • 46. E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation.
    Dumars KW; Fialko G; Larson E
    Birth Defects Orig Artic Ser; 1976; 12(5):97-104. PubMed ID: 953249
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Report on a case of Down's syndrome with mosaicism. Trisomy 21-normal, clearly mongoloid phenotype and normal iliac index in a newborn infant].
    De Prà M; Lunetta Q
    Minerva Pediatr; 1974 Jan; 26(2):78-81. PubMed ID: 4276194
    [No Abstract]   [Full Text] [Related]  

  • 48. [The chromosomal syndromes (author's transl)].
    Klein D
    Padiatr Padol Suppl; 1975; 4():1-31. PubMed ID: 127145
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother.
    Berg JM; Gardner HA; Gardner RJ; Goh EG; Markovic VD; Simpson NE; Worton RG
    J Med Genet; 1980 Apr; 17(2):144-8. PubMed ID: 6445984
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].
    D'Emma C; Crippa L; Delozier C; Michail E; Graber P
    J Genet Hum; 1982 Mar; 30(1):39-50. PubMed ID: 7130955
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Two balanced translocations in three generations of a pedigree: t(7;10) (q11;q22) and t(14;21) (14qter to cen to 21qter)1.
    Bass HN; Sparkes RS
    J Med Genet; 1979 Jun; 16(3):215-8. PubMed ID: 157395
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Heterochromatic regions of human chromosomes 1, 9, 16 and Y and the phenotype].
    Podgol'nikova OA; Grigor'eva NM; Bliumina MG
    Genetika; 1984 Mar; 20(3):496-500. PubMed ID: 6232170
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Inherited pericentric inversion of Y-chromosome with trisomy 21. A case report.
    Krishna Murthy DS; Murthy SK; Patel JK; Banker GN; Shah VC
    Ann Genet; 1989; 32(1):47-51. PubMed ID: 2526612
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Structural variation in human nitotic chromosomes.
    Leisti J
    Ann Acad Sci Fenn Biol; 1971; 179():1-69. PubMed ID: 4261167
    [No Abstract]   [Full Text] [Related]  

  • 56. [Trisomy 21. Report of 2 cases with unusual karyotypes].
    Sánchez O; de Marade S; Guerra D
    Invest Clin; 2001 Mar; 42(1):43-50. PubMed ID: 11294030
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Robertsonian translocation t dic (14p;22p) with regular trisomy 21: a possible interchromosomal effect?
    Farag TI; Krishna Murthy DS; Al-Awadi SA; Sundareshan TS; Ai-Othman SA; Mady SA; Redha MA
    Ann Genet; 1987; 30(3):189-92. PubMed ID: 2960263
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Human chromosome analysis: methodology and applications.
    Larson L
    Am J Med Technol; 1983 Oct; 49(10):687-98. PubMed ID: 6228140
    [TBL] [Abstract][Full Text] [Related]  

  • 59. The importance of chromosome analysis in Down's syndrome. A case report of a 21-21 translocation.
    Eber LM; Goodman RM
    Ohio State Med J; 1966 Jan; 62(1):40-3. PubMed ID: 4232315
    [No Abstract]   [Full Text] [Related]  

  • 60. Familial robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21.
    Mau UA; Petruch UR; Kaiser P; Eggermann T
    Eur J Hum Genet; 2000 Nov; 8(11):815-9. PubMed ID: 11093270
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 53.