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 *

94 related articles for article (PubMed ID: 5437582)

  • 21. A (15;18) translocation, unbalanced, 45 chromosomes. Human Genetic Mutant Cell Repository, Camden, N.J., identification No. GM-17.
    Cytogenet Cell Genet; 1973; 12(5):370-1. PubMed ID: 4780773
    [No Abstract]   [Full Text] [Related]  

  • 22. Cytogenetics in mentally defective children with anomalies: a controlled study.
    Summitt RL
    J Pediatr; 1969 Jan; 74(1):58-66. PubMed ID: 5782825
    [No Abstract]   [Full Text] [Related]  

  • 23. Inherited partial duplication of chromosome No. 15.
    Fujimoto A; Towner JW; Ebbin AJ; Kahlstrom EJ; Wilson MG
    J Med Genet; 1974 Sep; 11(3):287-91. PubMed ID: 4139262
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinico-neurological findings in connection of three chromosomal aberrations: an extra chromosome in group E, a D-C translocation and an unusually long B group chromosome.
    Iivanainen M; Gripenberg U
    Acta Neurol Scand; 1967; 43(S31):53-4. PubMed ID: 5583278
    [No Abstract]   [Full Text] [Related]  

  • 25. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM; Ornoy A; Rosenmann A; Kohn G
    Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Ring chromosome 18 in mother and daughter.
    Christensen KR; Friedrich U; Jacobsen P; Jensen K; Nielsen J; Tsuboi T
    J Ment Defic Res; 1970 Mar; 14(1):49-67. PubMed ID: 5534732
    [No Abstract]   [Full Text] [Related]  

  • 27. The supernumerary isochromosome 18 syndrome (+ 18pu).
    Condron CJ; Cantwell RJ; Kaufman RL; Brown SB; Warren RJ
    Birth Defects Orig Artic Ser; 1974; 10(10):36-42. PubMed ID: 4142590
    [No Abstract]   [Full Text] [Related]  

  • 28. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
    Miller JQ
    Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
    [No Abstract]   [Full Text] [Related]  

  • 29. Partial deletion of the long arm of chromosome E-18.
    Curran JP; al-Salihi FL; Allderdice PW
    Pediatrics; 1970 Nov; 46(5):721-9. PubMed ID: 5481073
    [No Abstract]   [Full Text] [Related]  

  • 30. [Familial D-E translocation].
    Meyer-Robisch M; Schwanitz G
    Acta Genet Med Gemellol (Roma); 1967 Oct; 16(4):365-75. PubMed ID: 5593928
    [No Abstract]   [Full Text] [Related]  

  • 31. Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.
    Fischer P; Golob E; Friedrich F; Kunze-Mühl E; Doleschel W; Aichmair H
    J Med Genet; 1970 Mar; 7(1):91-8. PubMed ID: 5480972
    [No Abstract]   [Full Text] [Related]  

  • 32. [Cardiovascular changes and clinical aspects of hypercalcemia in infants (Williams-Beuren syndrome)].
    Ebeling J; Bette L; Schiefer I
    Arch Kinderheilkd; 1969; 180(1):1-14. PubMed ID: 4191840
    [No Abstract]   [Full Text] [Related]  

  • 33. Partial F trisomy associated with familial F-13 translocation detected and identified by parental chromosome studies.
    Carrel RE; Sparkes RS; Wright SW
    J Pediatr; 1971 Apr; 78(4):664-72. PubMed ID: 5547823
    [No Abstract]   [Full Text] [Related]  

  • 34. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA; Mikel'saar AV; Mikel'saar RV
    Sov Genet; 1974 Jun; 8(5):651-7. PubMed ID: 4413436
    [No Abstract]   [Full Text] [Related]  

  • 35. Ring 13 chromosome with normal haptoglobin inheritance.
    Hollowell JG; Littlefield LG; Dharmkrong-AT A; Folger GM; Heath CW; Bloom GE
    J Med Genet; 1971 Jun; 8(2):222-6. PubMed ID: 5096545
    [No Abstract]   [Full Text] [Related]  

  • 36. t(2q-; Dq+) in a mentally retarded female child.
    Davison BC; Bedford J; Dunn W
    J Med Genet; 1970 Mar; 7(1):81-2. PubMed ID: 5480969
    [No Abstract]   [Full Text] [Related]  

  • 37. X-autosome translocation in normal mother and effectively 21-monosomic daughter.
    Summitt RL; Martens PR; Wilroy RS
    J Pediatr; 1974 Apr; 84(4):539-46. PubMed ID: 4834247
    [No Abstract]   [Full Text] [Related]  

  • 38. [The "Copenhagen chromosome" (syndrome of the small metacentric extra-chromosome)].
    Haberlandt W
    Arztl Forsch; 1971 Jul; 25(7):218-23. PubMed ID: 5109598
    [No Abstract]   [Full Text] [Related]  

  • 39. 18p - syndrome with a single central maxillary incisor.
    Dolan LM; Willson K; Wilson WG
    J Med Genet; 1981 Oct; 18(5):396-8. PubMed ID: 7328621
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ring chromosome 15:r(15). Identification by R banding.
    Stoll C; Juif JG; Luckel JC; Lausecker C
    Humangenetik; 1975; 27(3):259-62. PubMed ID: 50276
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.