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 *

154 related articles for article (PubMed ID: 14044305)

  • 21. [Genetic advice in Down's syndrome].
    Mikkelsen M
    Nord Med; 1971 Apr; 85(16):515. PubMed ID: 4252403
    [No Abstract]   [Full Text] [Related]  

  • 22. Autosomal trisomy in a chimpanzee: resemblance to Down's syndrome.
    McClure HM; Belden KH; Pieper WA; Jacobson CB
    Science; 1969 Sep; 165(3897):1010-2. PubMed ID: 4240970
    [TBL] [Abstract][Full Text] [Related]  

  • 23. THE ROLE OF CHROMOSOME TRANSLOCATION IN THE RECURRENCE RISK OF DOWN'S SYNDROME.
    PETERSEN CD; LUZZATTI L
    Pediatrics; 1965 Mar; 35():463-9. PubMed ID: 14258657
    [No Abstract]   [Full Text] [Related]  

  • 24. [Cytogenetic findings in patients with Down's syndrome].
    Cortés F; Alliende M; Curotto B
    Rev Chil Pediatr; 1990; 61(6):313-6. PubMed ID: 2152215
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. [FAMILY CONSULTATION IN MONGOLISM (DOWN'S SYNDROME)].
    LUEERS T
    Med Welt; 1965 Jan; 1():65-7. PubMed ID: 14272733
    [No Abstract]   [Full Text] [Related]  

  • 27. [Oxygen consumption of leukocytes in chromosome abnormalities. (Down's syndrome, ring chromosome 21, cri-du-chat syndrome, trisomy 18 and 22)].
    Heyne K
    Med Welt; 1980 Feb; 31(7):251-4. PubMed ID: 6445033
    [No Abstract]   [Full Text] [Related]  

  • 28. [Significance of the type of chromosome aberrations and biochemical disorders for diagnosis of Down's syndrome and the phenotype of partial trisomy 21].
    Mikiel-Kostyra K; Czerski P; Bartosz G; Sito A; Leyka W
    Pediatr Pol; 1980 Jan; 55(1):23-32. PubMed ID: 6445053
    [No Abstract]   [Full Text] [Related]  

  • 29. [Cytogenetic study and chromosome abnormalities of Alzheimer's disease and Down's syndrome].
    Asaka A
    Nihon Rinsho; 1988 Jul; 46(7):1502-7. PubMed ID: 2975715
    [No Abstract]   [Full Text] [Related]  

  • 30. Disorders associated with chromosomal aberrations. II. Down's syndrome (mongolism).
    SOLNITZKY O
    Georgetown Med Bull; 1962 May; 15():276-303. PubMed ID: 13914973
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. [Down's syndrome. Mongolism, trisomy 21].
    Mikkelsen M; Niebuhr E; Warburg M
    Ugeskr Laeger; 1971 Apr; 133(13):596-7. PubMed ID: 4252011
    [No Abstract]   [Full Text] [Related]  

  • 33. Detection of higher recurrence risk for age-dependent chromosome abnormalities with an application to trisomy G1. (Down's syndrome).
    Stene J
    Hum Hered; 1970; 20(1):112-22. PubMed ID: 4245815
    [No Abstract]   [Full Text] [Related]  

  • 34. [ENCIDENCE OF TRANSLOCATION AND TRISOMY 21 IN MONGOLOID IDIOTS (PRELIMINARY DATA)].
    PFEIFFER RA; HAHLER E
    Monatsschr Kinderheilkd (1902); 1964 Jun; 112():318-20. PubMed ID: 14234963
    [No Abstract]   [Full Text] [Related]  

  • 35. Structural rearrangements in the parents of children with primary trisomy 21.
    Couzin DA; Watt JL; Stephen GS
    J Med Genet; 1987 May; 24(5):280-2. PubMed ID: 2953898
    [TBL] [Abstract][Full Text] [Related]  

  • 36. BLOOD-SEROTONIN ACTIVITY IN TRISOMIC AND TRANSLOCATION DOWN'S SYNDROME.
    ROSNER F; ONG BH; PAINE RS; MAHANAND D
    Lancet; 1965 Jun; 1(7397):1191-3. PubMed ID: 14288558
    [No Abstract]   [Full Text] [Related]  

  • 37. MONGOLISM (DOWN'S SYNDROME) WITH ATYPICAL CLINICAL AND CYTOGENETIC FEATURES.
    SERGOVICH FR; VALENTINE GH; CARR DH; SOLTAN HC
    J Pediatr; 1964 Aug; 65():197-207. PubMed ID: 14198409
    [No Abstract]   [Full Text] [Related]  

  • 38. [THE PRINCIPLES OF FAMILIAL MONGOLISM].
    PFEIFFER RA
    Monatsschr Kinderheilkd (1902); 1964 Apr; 112():244-6. PubMed ID: 14203499
    [No Abstract]   [Full Text] [Related]  

  • 39. 46,XX,t(15;21)/47,XX,15p-,+21 mosaicism in a child with Down's syndrome.
    Lucas J; Le Mee F; Pluquailec K; Le Marec B; Journel H; Picard F
    Ann Genet; 1986; 29(2):104-6. PubMed ID: 2945509
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [ON THE PHENOTYPE OF CHROMOSOME ABNORMALITIES].
    PFEIFFER RA
    Z Mensch Vererb Konstitutionsl; 1964 Jun; 37():395-409. PubMed ID: 14251191
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.