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Journal Abstract Search

135 related items for PubMed ID: 6110234

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

  • 2. [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]

  • 3. "Newer" facial clefting syndromes.
    Gorlin RJ, Cervenka J, Cohen MM.
    Birth Defects Orig Artic Ser; 1977 May 15; 13(3B):1-9. PubMed ID: 329913
    [No Abstract] [Full Text] [Related]

  • 4. Interstitial deletion of chromosome 2.
    Marković S, Krstić M, Sulović V, Radojković Z, Adzić S.
    J Med Genet; 1985 Apr 15; 22(2):154-5. PubMed ID: 3989837
    [No Abstract] [Full Text] [Related]

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  • 9. Holoprosencephaly, ear abnormalities, congenital heart defect, and microphallus in a patient with 11q- mosaicism.
    Helmuth RA, Weaver DD, Wills ER.
    Am J Med Genet; 1989 Feb 15; 32(2):178-81. PubMed ID: 2494886
    [Abstract] [Full Text] [Related]

  • 10. [Syndrome of terminal deletion of the long arm of chromosome 4. Apropos of a personal case with a review of the literature].
    Frappaz D, Bourgeois J, Berthier JC, Laurent C, Bethenod M.
    Pediatrie; 1983 Jun 15; 38(4):261-70. PubMed ID: 6353348
    [Abstract] [Full Text] [Related]

  • 11. Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)].
    Al-Awadi SA, Farag TI, Usha R, el-Khalifa MY, Sundareshan TS, Al-Othman SA.
    Am J Med Genet; 1986 Apr 15; 23(4):931-3. PubMed ID: 3963055
    [Abstract] [Full Text] [Related]

  • 12. O--short stature with abnormalities of the cranium and limbs.
    Jorgenson RJ.
    Birth Defects Orig Artic Ser; 1974 Apr 15; 10(5):249-51. PubMed ID: 4469995
    [No Abstract] [Full Text] [Related]

  • 13. [Wolf syndrome. Apropos of 2 cases].
    García González P, Pedraz García C, Merino Marcos L, Salazar Veloz J, Escudero Bueno G, Salazar Villalobos V.
    An Esp Pediatr; 1983 Feb 15; 18(2):113-7. PubMed ID: 6881733
    [Abstract] [Full Text] [Related]

  • 14. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
    Leichtman LG, Zackowski JL, Storto PD, Newlin A.
    Am J Med Genet; 1996 Jun 14; 63(3):434-7. PubMed ID: 8737648
    [Abstract] [Full Text] [Related]

  • 15. Hypoplastic pelvis in association with multiple anomalies.
    Baden M, Ortiz A, Goyette RE, Kirks DR.
    Pediatrics; 1974 Feb 14; 53(2):270-3. PubMed ID: 4149572
    [No Abstract] [Full Text] [Related]

  • 16. Opitz GBBB syndrome and the 22q11.2 deletion.
    Lacassie Y, Arriaza MI.
    Am J Med Genet; 1996 Mar 29; 62(3):318. PubMed ID: 8882795
    [No Abstract] [Full Text] [Related]

  • 17. Interstitial deletion 2q31 leads to q33.
    Buchanan PD, Rhodes RL, Stevenson CE.
    Am J Med Genet; 1983 May 29; 15(1):121-6. PubMed ID: 6683075
    [Abstract] [Full Text] [Related]

  • 18. Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.
    Saal HM, King LJ, Zimmerman D, Johnson RC, Carr AG, Samango-Sprouse CA, Stanley W.
    Am J Med Genet; 1996 Dec 30; 66(4):373-7. PubMed ID: 8989454
    [Abstract] [Full Text] [Related]

  • 19. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
    Taysi K, Dengler DR, Jones LA, Heersma JR.
    Ann Genet; 1981 Dec 30; 24(4):245-7. PubMed ID: 7036843
    [No Abstract] [Full Text] [Related]

  • 20. Multiple congenital anomalies, thymic dysplasia, severe congenital heart disease, and oligosyndactyly with a deletion of the short arm of chromosome 5.
    Taylor MJ, Josifek K.
    Am J Med Genet; 1981 Dec 30; 9(1):5-11. PubMed ID: 6264787
    [Abstract] [Full Text] [Related]

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