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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

281 related items for PubMed ID: 4142400

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
    Vigfusson NV, Kapstafer KJ, Lloyd MA.
    Am J Med Genet; 1980; 7(3):383-9. PubMed ID: 7468662
    [Abstract] [Full Text] [Related]

  • 23.
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  • 24. Gross anatomical studies of a newborn infant with the Meckel syndrome.
    Pettersen JC.
    Am J Med Genet; 1984 Aug; 18(4):649-59. PubMed ID: 6486165
    [Abstract] [Full Text] [Related]

  • 25. [Potter's syndrome and polycystic kidney in the newborn].
    Pasquier B, Couderc P, Bost M, Rambaud P.
    Sem Hop; 1971 Dec 08; 47(49):2779-88. PubMed ID: 4335740
    [No Abstract] [Full Text] [Related]

  • 26.
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  • 27. [Hereditary kidney diseases in children (a review of the literature)].
    Degtiareva EM.
    Vopr Okhr Materin Det; 1973 Mar 08; 18(3):36-40. PubMed ID: 4585577
    [No Abstract] [Full Text] [Related]

  • 28. Malformative syndrome with ring chromosome 13.
    Fryns JP, Deoover J, Van den Berghe H.
    Humangenetik; 1974 Mar 08; 24(3):235-40. PubMed ID: 4140834
    [No Abstract] [Full Text] [Related]

  • 29.
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  • 30. A case of chromosome abnormality (46, XX, Gq+) with congenital heart disease and leprechaunism.
    Iwaski H, Abe M, Nawate G, Kato H.
    Jinrui Idengaku Zasshi; 1974 Jun 08; 19(1):82-3. PubMed ID: 4476865
    [No Abstract] [Full Text] [Related]

  • 31.
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  • 32. [Three new cases of Meckel's syndrome or Gruber's splanchnocystic dysencephaly in siblings. Anatomo-pathologic and cytogenetic study. Nosologic discussion].
    Naffah J, Ghosn G, Gharios N.
    Arch Fr Pediatr; 1972 Dec 08; 29(10):1069-81. PubMed ID: 4662280
    [No Abstract] [Full Text] [Related]

  • 33.
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  • 34.
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  • 35.
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  • 36. [9p monosomy. About a new case. Clinical and cytogenetic study (author's transl)].
    Lajarrige C, Bouquier JJ, Ronayette D, Tchertoff C, Faugeras C, Barthe D, Laleu J.
    Ann Pediatr (Paris); 1979 Nov 08; 26(9):631-6. PubMed ID: 555637
    [No Abstract] [Full Text] [Related]

  • 37.
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  • 38. [Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].
    Dutrillaux B, Laurent C, Robert JM, Lejeune J.
    Cytogenet Cell Genet; 1973 Nov 08; 12(4):245-53. PubMed ID: 4752866
    [No Abstract] [Full Text] [Related]

  • 39.
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  • 40. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
    Murthy DS, Murthy SK, Banker GJ, Patel AJ.
    Indian Pediatr; 1991 May 08; 28(5):546-9. PubMed ID: 1684352
    [No Abstract] [Full Text] [Related]

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