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Journal Abstract Search

205 related items for PubMed ID: 14227326

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  • 3. TRIPLE CHROMOSOMAL MOSAICISM IN A JAPANESE CHILD WITH DOWN'S SYNDROME.
    TONOMURA A, KURITA T.
    Acta Genet Stat Med; 1964; 14():67-75. PubMed ID: 14159882
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  • 10. FAMILIAL DOWN'S SYNDROME WITH UNDETECTED TRANSLOCATION.
    DAY RW, MILES CP.
    J Pediatr; 1965 Sep; 67():399-409. PubMed ID: 14339398
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  • 13. 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 Sep; 75(4):545-54. PubMed ID: 4246134
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  • 14. Radiological features of the most common autosomal disorders: trisomy 21-22 (mongolism or Down's syndrome), trisomy 18, trisomy 13-15, and the cri du chat syndrome.
    James AE, Merz T, Janower ML, Dorst JP.
    Clin Radiol; 1971 Oct; 22(4):417-33. PubMed ID: 4257566
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  • 17. [MONGOL CHILD-MOSAIC PARENT. STUDY OF 2 FAMILIES].
    FERRIER S.
    J Genet Hum; 1964 Dec; 13():315-36. PubMed ID: 14269571
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  • 19. CLOSED METOPIC SUTURE WITH TRIGONOCEPHALY IN DOWN'S SYNDROME.
    DEMYER W, PALMER C.
    Neurology; 1965 Aug; 15():756-60. PubMed ID: 14315300
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  • 20. Down's syndrome. I. Cytogenetics.
    Maximilian C, Duca D, Pop T, Toncescu N, Ioan D.
    Endocrinologie; 1980 Aug; 18(4):273-5. PubMed ID: 6451918
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