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Journal Abstract Search

242 related items for PubMed ID: 6974525

  • 21. Terminal deletion of 6p: report of a new case.
    Plaja A, Vidal R, Soriano D, Bou X, Vendrell T, Mediano C, Pueyo JM, Labraña X, Sarret E.
    Ann Genet; 1994; 37(4):196-9. PubMed ID: 7710255
    [Abstract] [Full Text] [Related]

  • 22. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML, Pai GS, Wilkes B, Lebel RR.
    Am J Med Genet; 2001 Aug 15; 102(3):237-42. PubMed ID: 11484200
    [Abstract] [Full Text] [Related]

  • 23. Deletions of the long arm of chromosome 6: two new cases and review of the literature.
    Young RS, Fidone GS, Reider-Garcia PA, Hansen KL, McCombs JL, Moore CM.
    Am J Med Genet; 1985 Jan 15; 20(1):21-9. PubMed ID: 3881954
    [Abstract] [Full Text] [Related]

  • 24. [Deletion of the long arm of the Y chromosome and multiple malformations. Description of a case].
    Scherini A, Sangermani R, Elli P.
    Minerva Pediatr; 1979 May 15; 31(9):729-31. PubMed ID: 460118
    [No Abstract] [Full Text] [Related]

  • 25. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32).
    Martin-Pont B, Pilczer C, Dandine M, Tamboise A.
    Ann Genet; 1985 May 15; 28(4):251-3. PubMed ID: 3879441
    [Abstract] [Full Text] [Related]

  • 26. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP, Heck LJ, Carter GA, Flom JO.
    Am J Med Genet; 1985 Dec 15; 22(4):685-94. PubMed ID: 4073121
    [Abstract] [Full Text] [Related]

  • 27. The 4q-Syndrome.
    Strehle EM, Ahmed OA, Hameed M, Russell A.
    Genet Couns; 2001 Dec 15; 12(4):327-39. PubMed ID: 11837601
    [Abstract] [Full Text] [Related]

  • 28. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA, Higgins RR, Mendelsohn NJ, Casey TM, Steinberger J, Mammel MC, Wiesner GL.
    Am J Med Genet; 1995 May 22; 57(1):52-6. PubMed ID: 7645598
    [Abstract] [Full Text] [Related]

  • 29. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
    Young RS, Palmer CG, Bender HA, Weaver DD, Hodes ME.
    Am J Med Genet; 1982 May 22; 12(1):103-7. PubMed ID: 7091193
    [No Abstract] [Full Text] [Related]

  • 30. Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases.
    Young RS, Weaver DD, Kukolich MK, Heerema NA, Palmer CG, Kawira EL, Bender HA.
    Am J Med Genet; 1984 Feb 22; 17(2):437-50. PubMed ID: 6199974
    [Abstract] [Full Text] [Related]

  • 31. Brief clinical report: the del(4) (q31) syndrome- a recognizable disorder with atypical Robin malformation sequence.
    Davis JM, Clarren SK, Salk DJ.
    Am J Med Genet; 1981 Feb 22; 9(2):113-7. PubMed ID: 7258224
    [Abstract] [Full Text] [Related]

  • 32. 11q- syndrome: three cases and a review of the literature.
    Leegte B, Kerstjens-Frederikse WS, Deelstra K, Begeer JH, van Essen AJ.
    Genet Couns; 1999 Feb 22; 10(3):305-13. PubMed ID: 10546104
    [Abstract] [Full Text] [Related]

  • 33. Terminal deletion 4q in a severely retarded boy.
    de Michelena MI, Campos PJ.
    Am J Med Genet; 1989 Jun 22; 33(2):228-30. PubMed ID: 2764033
    [Abstract] [Full Text] [Related]

  • 34. Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype.
    Tsai CH, Van Dyke DL, Feldman GL.
    Am J Med Genet; 1999 Feb 12; 82(4):336-9. PubMed ID: 10051168
    [Abstract] [Full Text] [Related]

  • 35. Partial monosomy of the long arm of chromosome 11 in a severely affected child.
    Lee ML, Sciorra LJ.
    Ann Genet; 1981 Feb 12; 24(1):51-3. PubMed ID: 6971620
    [Abstract] [Full Text] [Related]

  • 36. Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant.
    Donahue ML, Ryan RM.
    Am J Med Genet; 1995 Mar 13; 56(1):97-100. PubMed ID: 7747796
    [Abstract] [Full Text] [Related]

  • 37. Infant with del(3) (p25-pter): karyotype-phenotype correlation and review of previously reported cases.
    Nienhaus H, Mau U, Zang KD.
    Am J Med Genet; 1992 Nov 15; 44(5):573-5. PubMed ID: 1481811
    [Abstract] [Full Text] [Related]

  • 38. Familial t(4;13) with abnormal offspring in three generations.
    Najafzadeh TM, Littman VA, Dumars KW.
    Am J Med Genet; 1983 Sep 15; 16(1):15-22. PubMed ID: 6638065
    [Abstract] [Full Text] [Related]

  • 39. [Deletion of the short arm of chromosome 4].
    Hurgoiu V, Lazăr Garoiu F, Giurgiuman M, Rusu S.
    Rev Pediatr Obstet Ginecol Pediatr; 1980 Sep 15; 29(3):243-8. PubMed ID: 6110234
    [No Abstract] [Full Text] [Related]

  • 40. Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysis.
    Lukusa T, Smeets E, Vermeesch JR, Fryns JP.
    Genet Couns; 2002 Sep 15; 13(4):417-25. PubMed ID: 12558112
    [Abstract] [Full Text] [Related]

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