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Journal Abstract Search

245 related items for PubMed ID: 47133

  • 1. Letter: Mongolism by tertiary trisomy.
    Chaganti RS, Morillo-Cucci G, Degnan M, German J.
    Lancet; 1975 Mar 22; 1(7908):698-9. PubMed ID: 47133
    [No Abstract] [Full Text] [Related]

  • 2. Trisomy and D/G translocation mongolism in brothers.
    Ingalls TH, Henry TA.
    N Engl J Med; 1968 Jan 04; 278(1):10-4. PubMed ID: 4229204
    [No Abstract] [Full Text] [Related]

  • 3. 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 04; 11(3):207-13. PubMed ID: 138497
    [Abstract] [Full Text] [Related]

  • 4. Retardation in a child with an extra submetacentric chromosome fragment and partial mongolism.
    Dekaban AS, Zelson J.
    J Ment Defic Res; 1968 Sep 04; 12(3):216-25. PubMed ID: 4235427
    [No Abstract] [Full Text] [Related]

  • 5. Trisomy-21 in mother and child. Report of a case.
    Friedman JM, Sternberg WH, Varela M, Barclay DL.
    Obstet Gynecol; 1970 Nov 04; 36(5):731-4. PubMed ID: 4248734
    [No Abstract] [Full Text] [Related]

  • 6. Familial enlargement of the short arm of a small acrocentric chromosome.
    Vamos-Hurwitz E, Arya S, Boggs TR, Nichols WW.
    Hereditas; 1967 Nov 04; 57(1):185-97. PubMed ID: 4229893
    [No Abstract] [Full Text] [Related]

  • 7. Partial trisomy in a child with features suggesting mongolism.
    Kumbnani HK, Pfeiffer RA.
    J Med Genet; 1969 Jun 04; 6(2):201-5. PubMed ID: 4240723
    [No Abstract] [Full Text] [Related]

  • 8. Trisomy 18 and 21 in two siblings.
    Crandall BF, Ebbin AJ.
    Clin Genet; 1973 Jun 04; 4(6):517-9. PubMed ID: 4274618
    [No Abstract] [Full Text] [Related]

  • 9. Chromosome anomalies in mongolism.
    Atkins L.
    N Engl J Med; 1968 Mar 07; 278(10):565-6. PubMed ID: 4230020
    [No Abstract] [Full Text] [Related]

  • 10. [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]

  • 11. [Identification of numerical and structural anomalies of human G-group-chromosomes using the pankreatin-Giemsa-Banding-pattern].
    Müller W, Rosenkranz W.
    Klin Padiatr; 1972 Jul 24; 184(4):265-71. PubMed ID: 4117041
    [No Abstract] [Full Text] [Related]

  • 12. Identification by fluorescence of apparently extra human F chromosomes as G chromosomes with giant satellites.
    Wahlström J.
    Hereditas; 1972 Jul 24; 71(1):154-7. PubMed ID: 4281766
    [No Abstract] [Full Text] [Related]

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  • 14. [Report on a case of Down's syndrome with mosaicism. Trisomy 21-normal, clearly mongoloid phenotype and normal iliac index in a newborn infant].
    De Prà M, Lunetta Q.
    Minerva Pediatr; 1974 Jan 28; 26(2):78-81. PubMed ID: 4276194
    [No Abstract] [Full Text] [Related]

  • 15. New techniques in the study of human chromosomes: methods and applications.
    Dutrillaux B, Lejeune J.
    Adv Hum Genet; 1975 Jan 28; 5():119-56. PubMed ID: 48327
    [No Abstract] [Full Text] [Related]

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  • 18. Down's syndrome transmitted through maternal mosaicism.
    Aarskog D.
    Acta Paediatr Scand; 1969 Nov 28; 58(6):609-14. PubMed ID: 4244880
    [No Abstract] [Full Text] [Related]

  • 19. Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis.
    Caspersson T, Hultén M, Lindsten J, Therkelsen AJ, Zech L.
    Hereditas; 1971 Nov 28; 67(2):213-20. PubMed ID: 4142007
    [No Abstract] [Full Text] [Related]

  • 20. [Quantitative multienzymatic deficiency and chromosome malsegregation: patients with trisomy 21 and their parents].
    Grozdea J, Colombies P, Verdier J.
    Nouv Presse Med; 1973 May 12; 2(19):1289-91. PubMed ID: 4268234
    [No Abstract] [Full Text] [Related]

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