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.


PUBMED FOR HANDHELDS

Journal Abstract Search


196 related items for PubMed ID: 6971601

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

  • 22. Trisomy 14q-.
    Fawcett WA, McCord WK, Francke U.
    Birth Defects Orig Artic Ser; 1975; 11(5):223-8. PubMed ID: 1218218
    [Abstract] [Full Text] [Related]

  • 23. Abnormal chromosome 9 in a neonate program. Report of three cases.
    Nakamura Y, Sato E, Sakai K, Sakuma S, Hashimoto T, Sindou S.
    Arch Pathol Lab Med; 1990 Feb; 114(2):185-7. PubMed ID: 2302035
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. [Numerical and structural anomalies of chromosome no. 18 (author's transl)].
    Aksu F, Mietens C, Scholz W.
    Klin Padiatr; 1976 May; 188(3):220-32. PubMed ID: 945418
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Familial translocation 2;17 with partial trisomy 2q32 leads to 2qter.
    Giliberti P, Celona A, Della Pietra M, De Masi RV, Fioretti G, Pagano L, Renda S, Vetrella A, Ventruto V.
    Ann Genet; 1980 May; 23(4):249-50. PubMed ID: 6971607
    [Abstract] [Full Text] [Related]

  • 31. [A small supernumerary metacentric chromosome: interprétation test (author's transl)].
    Ayraud N, Noel B, Llyod M, Letourneau J, Martinon J.
    J Genet Hum; 1976 Jun; 24(2):81-93. PubMed ID: 965953
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Partial trisomy 9q resulting from a familial translocation t(9;16)(q32;q24).
    Soltan HC, Jung JH, Pyatt Z, Singh RP.
    Clin Genet; 1984 May; 25(5):449-54. PubMed ID: 6723106
    [Abstract] [Full Text] [Related]

  • 34. [12 p trisomy. A new case (author's transl)].
    Kubryk N, Prieur M, Borde M.
    Ann Pediatr (Paris); 1980 Dec; 27(10):695-9. PubMed ID: 7212558
    [No Abstract] [Full Text] [Related]

  • 35. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M, Hemly NA, Zaki MS.
    Genet Couns; 2007 Dec; 18(2):217-26. PubMed ID: 17710874
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. [Clinical and cytogenetic study of a case of trisomy 1q with familial translocation t (1; 5) (q 42; p 15.3) (author's transl)].
    Duillo MT, de Toni T, Cavaliere G, Bava GL, Arslanian A, Bonioli E, Vianello MG.
    Pathologica; 1979 Dec; 71(1012):223-34. PubMed ID: 471543
    [No Abstract] [Full Text] [Related]

  • 39. Trisomy 6q25 leads to 6qter in two sisters resulting from maternal 6;11 translocation.
    Clark CE, Cowell HR, Telfer MA, Casey PA.
    Am J Med Genet; 1980 Dec; 5(2):171-8. PubMed ID: 7395910
    [Abstract] [Full Text] [Related]

  • 40. A case of Edward's syndrome with pseudodicentric isochromosome 18: 46,XY,i dic(18) (p11::p11).
    Fioretti G, Stabile M, Pagano L, Rinaldi A, Rolando D, Trapassi C, de Tollis G, Ventruto V.
    Ann Genet; 1982 Dec; 25(2):116-8. PubMed ID: 6984627
    [No Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 10.