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PUBMED FOR HANDHELDS

Journal Abstract Search

113 related items for PubMed ID: 4157662

  • 1. Biochemical consequences of supernumerary chromosome subtype in mongolism.
    Pozsonyi J.
    Am J Ment Defic; 1965 Sep; 70(2):213-7. PubMed ID: 4157662
    [No Abstract] [Full Text] [Related]

  • 2. [Biochemical maturation of the catecholamine system during growth].
    Blancher G.
    Arch Fr Pediatr; 1974 Sep; 31(2):263-70. PubMed ID: 4277137
    [No Abstract] [Full Text] [Related]

  • 3. [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 15; 31(7):251-4. PubMed ID: 6445033
    [No Abstract] [Full Text] [Related]

  • 4. Endocrine investigations into mongolism.
    Reiss M, Wakoh T, Hillman JC, Pearse JJ, Daley N, Reiss JM.
    Am J Ment Defic; 1965 Sep 15; 70(2):204-12. PubMed ID: 4157494
    [No Abstract] [Full Text] [Related]

  • 5. [On cytogenetics of mongolism with special reference to the familial form].
    Heinz HA.
    Verh Dtsch Ges Pathol; 1965 Sep 15; 49():333-8. PubMed ID: 4160575
    [No Abstract] [Full Text] [Related]

  • 6. [Trisomy 21 associated with gonosomic mongolism].
    Duillo MT, Serra G.
    Minerva Pediatr; 1969 Nov 24; 21(47):2196-201. PubMed ID: 4249915
    [No Abstract] [Full Text] [Related]

  • 7. Reproduction in down's syndrome (mongolism): chromosomal study of mother and normal child.
    Tagher P, Reisman LE.
    Obstet Gynecol; 1966 Feb 24; 27(2):182-4. PubMed ID: 4222376
    [No Abstract] [Full Text] [Related]

  • 8. [On possible relations between cytogenetic anomalies and cytochemical alterations. Alkaline leukophosphatase in mongolism].
    Bertolotti E, Loiodice G, Quazza GF, Vianello MG.
    Minerva Pediatr; 1965 Nov 03; 17(33):1729-32. PubMed ID: 4222497
    [No Abstract] [Full Text] [Related]

  • 9. [Chromosome conditioned oligophrenic states (mongolism, Patau syndrome, Edwards syndrome)].
    Koch G.
    Folia Clin Int (Barc); 1965 Dec 03; 15(12):555-64. PubMed ID: 4222586
    [No Abstract] [Full Text] [Related]

  • 10. [The intelligence level in the chromosome aberrations affecting autosomes].
    Moor L.
    Rev Neuropsychiatr Infant; 1970 Dec 03; 18(12):943-66. PubMed ID: 4251821
    [No Abstract] [Full Text] [Related]

  • 11. [Children with chromosome abnormalities in a pediatric department].
    Nielsen J, Friedrich U, Holm V, Sveinsson S.
    Ugeskr Laeger; 1973 Feb 19; 135(8):408-15. PubMed ID: 4265917
    [No Abstract] [Full Text] [Related]

  • 12. Neurologic aspects of typical and atypical Down's syndrome.
    Paulson GW, Nance W, Son C.
    Neurology; 1968 Mar 19; 18(3):305-6. PubMed ID: 4231810
    [No Abstract] [Full Text] [Related]

  • 13. CYTOGENETICS IN MONGOLISM. A REVIEW OF LITERATURE AND PERSONAL INVESTIGATION.
    AULA P, HJELT L.
    Ann Paediatr Fenn; 1964 Mar 19; 10():13-23. PubMed ID: 14116180
    [No Abstract] [Full Text] [Related]

  • 14. [CHROMOSOME ABNORMALITIES IN PEDIATRICS (WITH THE EXCEPTION OF MONGOLISM AND SEX ANOMALIES)].
    TABATA T.
    Sogo Igaku; 1964 Feb 19; 21():101-5. PubMed ID: 14136973
    [No Abstract] [Full Text] [Related]

  • 15. [THE PRINCIPLES OF FAMILIAL MONGOLISM].
    PFEIFFER RA.
    Monatsschr Kinderheilkd (1902); 1964 Apr 19; 112():244-6. PubMed ID: 14203499
    [No Abstract] [Full Text] [Related]

  • 16. [Cutaneous papillary reliefs of the hand: methods of study and applications in pediatrics].
    Schwarzenberg TL, Lapi AS, Canibus R, Mencarini L, Mancini G.
    Arch Ital Pediatr Pueric; 1968 Apr 19; 26(2):81-131. PubMed ID: 4243061
    [No Abstract] [Full Text] [Related]

  • 17. [Serum proteins in trisomy 21].
    Bouchard M, Fortin B, Desgagné A.
    Laval Med; 1968 Mar 19; 39(3):215-21. PubMed ID: 4247353
    [No Abstract] [Full Text] [Related]

  • 18. Unusual chromosome aberrations in 3 children with Down syndrome.
    Osztovics M, Tóth S, Wilhelm O.
    Acta Paediatr Acad Sci Hung; 1982 Mar 19; 23(3):283-9. PubMed ID: 6217717
    [Abstract] [Full Text] [Related]

  • 19. [Trisomy 13 syndrome (Patau syndrome), trisomy 18 syndrome (Edwards syndrome), Down syndrome (trisomy 21 syndrome), Turner syndrome (XO gonadal dysgenesis)].
    Harada N, Niikawa N.
    Ryoikibetsu Shokogun Shirizu; 1996 Mar 19; (15):198-201. PubMed ID: 9047985
    [No Abstract] [Full Text] [Related]

  • 20. [Thyroid autoimmunity and chromosome aberration].
    Dallaire L, Kingsmill Flynn D.
    Union Med Can; 1967 Nov 19; 96(11):1371-5. PubMed ID: 4235851
    [No Abstract] [Full Text] [Related]

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