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 *

203 related articles for article (PubMed ID: 3587191)

  • 41. Familial D-D translocation. A family showing transmission through three generations; a case with multiple congenital malformations, and a case of regular 21-trisomic Down's syndrome.
    Visfeldt J
    Acta Pathol Microbiol Scand; 1969; 75(4):545-54. PubMed ID: 4246134
    [No Abstract]   [Full Text] [Related]  

  • 42. [Ring chromosome D13-case history and survey (author's transl)].
    Zink U; Rix R; Grosse KP; Schwanitz G
    Klin Padiatr; 1973 May; 185(3):192-7. PubMed ID: 4795573
    [No Abstract]   [Full Text] [Related]  

  • 43. The Cornelia de Lange syndrome: clinical and cytogenetic interpretations.
    Payne HW; Maeda WK
    Can Med Assoc J; 1965 Sep; 93(11):577-86. PubMed ID: 5825977
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Trisomy 18-Edwards syndrome: a report of three patients.
    Ejiwumni AB; Msamati BC
    Cent Afr J Med; 1993 May; 39(5):105-9. PubMed ID: 8131193
    [No Abstract]   [Full Text] [Related]  

  • 45. [Multiple abnormalities in a newborn infant with a D1ring chromosome].
    Biles AR; Lüers T; Sperling K
    Med Welt; 1969 Aug; 33():1771-5. PubMed ID: 5357975
    [No Abstract]   [Full Text] [Related]  

  • 46. [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]  

  • 47. Duplication 3q syndrome: molecular delineation of the critical region.
    Aqua MS; Rizzu P; Lindsay EA; Shaffer LG; Zackai EH; Overhauser J; Baldini A
    Am J Med Genet; 1995 Jan; 55(1):33-7. PubMed ID: 7702094
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The Brachmann-De Lange syndrome: a case report.
    Kaplan B
    S Afr Med J; 1968 Oct; 42(41):1118-9. PubMed ID: 5749742
    [No Abstract]   [Full Text] [Related]  

  • 49. Osseous malformations associated with chromosome abnormalities.
    Weiss L; Reynolds WA
    Orthop Clin North Am; 1972 Nov; 3(3):713-32. PubMed ID: 4264453
    [No Abstract]   [Full Text] [Related]  

  • 50. [Caudal block and sedation for bilateral herniorrhaphy in an infant with Cornelia de Lange syndrome].
    del Rio ER; Cordero Luna D; Vásquez Montes MT; Chávez Ramírez MA; Rodríguez Pérez MV; Cruz-Villaseñor JA; Rodríguez Aranda E; Olvera Durán JA
    Rev Esp Anestesiol Reanim; 2004; 51(7):403-4. PubMed ID: 15495641
    [No Abstract]   [Full Text] [Related]  

  • 51. A practical application of fluorescent in situ hybridization to the Wolf-Hirschhorn syndrome.
    Fagan K; Colley P; Partington M
    Pediatrics; 1994 May; 93(5):826-7. PubMed ID: 8165089
    [No Abstract]   [Full Text] [Related]  

  • 52. A distinct multiple congenital anomalies syndrome associated with distal 5q deletion (q35.1qter).
    Kleczkowska A; Fryns JP; van den Berghe H
    Ann Genet; 1993; 36(2):126-8. PubMed ID: 8215219
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [A patient with ring chromosome 13].
    Hammond A; Bijlsma JB
    Ned Tijdschr Geneeskd; 1981 May; 125(19):752-5. PubMed ID: 7242723
    [No Abstract]   [Full Text] [Related]  

  • 54. A girl with inverted triplication of chromosome 3q25.3 --> q29 and multiple congenital anomalies consistent with 3q duplication syndrome.
    Ounap K; Ilus T; Bartsch O
    Am J Med Genet A; 2005 May; 134(4):434-8. PubMed ID: 15793836
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Syndrome 4p-].
    Subrt I; Blehová B
    Cesk Pediatr; 1973 Feb; 28(2):75-7. PubMed ID: 4686581
    [No Abstract]   [Full Text] [Related]  

  • 56. [Partial deletion of the short arm of chromosome 4 (the Wolf-Hirschhorn syndrome) with reference to the neurological and electroencephalographic aspects].
    Bonaventura F; Adamoli P; Bernardini E; Branchi M; Siani A; Bonora G
    Pediatr Med Chir; 1994; 16(4):393-8. PubMed ID: 7816704
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Intrauterine diagnosis of a chromosome translocation].
    Aula P; Karjalainen O; Leisti J
    Duodecim; 1971; 87(20):1372-7. PubMed ID: 5115096
    [No Abstract]   [Full Text] [Related]  

  • 58. [Similarity between the syndrome of partial trisomy of the long arm of chromosome 3 and the Cornelia de Lange syndrome].
    Polívková Z; Kucerová M; Dolanská M; Hresová M; Kofer J
    Cesk Pediatr; 1988 Dec; 43(12):723-6. PubMed ID: 3250742
    [No Abstract]   [Full Text] [Related]  

  • 59. [The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].
    Gilgenkrantz S; Marchal C; Neimann N
    Ann Genet; 1968 Mar; 11(1):17-21. PubMed ID: 5301751
    [No Abstract]   [Full Text] [Related]  

  • 60. [Syndrome of ring deletion of group E chromosome in a female infant].
    Baniowski A; Kleczkowska A; Kubień E; Sokolowski J
    Pediatr Pol; 1971 Sep; 46(9):1167-70. PubMed ID: 5114250
    [No Abstract]   [Full Text] [Related]  

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