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 *

140 related articles for article (PubMed ID: 126210)

  • 21. Translocation and trisomic Down's syndrome in a family with a familial D-G translocation.
    Zizka J
    Cytologia (Tokyo); 1969 Sep; 34(3):423-8. PubMed ID: 4244707
    [No Abstract]   [Full Text] [Related]  

  • 22. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome.
    Kitsiou-Tzeli S; Hallett JJ; Atkins L; Latt SA; Holmes LB
    Am J Med Genet; 1984 Aug; 18(4):725-9. PubMed ID: 6237580
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Unstable telocentric chromosome produced after centric misdivision of a 21q/21q translocated element.
    Guanti G; Maritato F
    Hum Genet; 1978 Dec; 45(3):355-62. PubMed ID: 153887
    [TBL] [Abstract][Full Text] [Related]  

  • 25. De novo translocation Down's syndrome: risk of recurrence of Down's syndrome.
    Gardner RJ; Veale AM
    Clin Genet; 1974; 6(3):160-4. PubMed ID: 4279152
    [No Abstract]   [Full Text] [Related]  

  • 26. Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype.
    Hagemeijer A; Smit EM
    Hum Genet; 1977 Aug; 38(1):15-23. PubMed ID: 143443
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Familial balanced translocation 4p+/17q- as a suggested cause of primary trisomy-21 Down's syndrome.
    Oikawa K; Trent M; Lebovitz R
    Arch Dis Child; 1977 Nov; 52(11):890-3. PubMed ID: 145829
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Three interesting cases of Down's syndrome.
    Pérez-Castillo A; Del Mazo J; Abrisqueta JA
    Ann Genet; 1983; 26(2):123-8. PubMed ID: 6225371
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21.
    Pfeiffer RA; Kessel EK; Soer KH
    Clin Genet; 1977 Mar; 11(3):207-13. PubMed ID: 138497
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 21-22 translocation Down's syndromea family with unusual segregating patterns.
    Yang SJ; Rosenberg HS
    Am J Hum Genet; 1969 May; 21(3):248-51. PubMed ID: 4240105
    [No Abstract]   [Full Text] [Related]  

  • 31. Indophenol-oxidase in patients with Down's syndrome due to simple trisomy and to translocation 21/22.
    Kedziora J; Rozynkowa D; Kopff M; Jeske J
    Hum Genet; 1976 Sep; 34(1):9-12. PubMed ID: 184031
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Maternal transmission of translocation 2;21 associated with Down's syndrome.
    Kotwaliwale SV; Dicholkar VV; Motashaw ND
    J Med Genet; 1991 Jun; 28(6):415-6. PubMed ID: 1831234
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Karyotypic analysis of 150 cases of Down's Syndrome in Iraq.
    Ferman A; Shakir A
    J Ment Defic Res; 1976 Jun; 20(2):83-7. PubMed ID: 133247
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Inherited t2q-/15q+ translocation and Down's syndrome.
    Stoll C; Kuss JJ; Schneegans E
    Clin Genet; 1976 Jan; 9(1):5-7. PubMed ID: 129308
    [No Abstract]   [Full Text] [Related]  

  • 36. Dermatoglyphic peculiarities in Down's syndrome detection of mosaicism and balanced translocation carriers.
    Rodewald A; Zang KD; Zankl H; Zankl M
    Hum Genet Suppl; 1981; 2():41-56. PubMed ID: 6218140
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cytogenetic studies of a family with trisomy 21 mosaicism in two successive generations as the cause of Down's syndrome.
    Werner W; Herrmann FH; John B
    Hum Genet; 1982; 60(2):202-4. PubMed ID: 6210621
    [No Abstract]   [Full Text] [Related]  

  • 38. [Familial occurrence of translocation (13q 14q) and 14q 21q)].
    Czerski P; Rogóyski A; Stolarska A
    Pediatr Pol; 1977 Apr; 52(4):429-35. PubMed ID: 141033
    [No Abstract]   [Full Text] [Related]  

  • 39. A t(5p-;21q+) translocation in a family with Down syndrome.
    Neu RL; DeGeorge FV; Gardner LI
    Clin Genet; 1977 Aug; 12(2):111-3. PubMed ID: 142593
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Banding identification of chromosomal abnormalities in four patients: ring (6), translocation (2q-;15q+), translocation (21q;21q) and deletion (22q-).
    Wurster-Hill DH; Hoefnagel D
    J Ment Defic Res; 1975 Jun; 19(2):145-50. PubMed ID: 127842
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.