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210 related items for PubMed ID: 1519644

  • 1. 7p deletion syndrome: an adult with mild manifestations.
    Grebe TA, Stevens MA, Byrne-Essif K, Cassidy SB.
    Am J Med Genet; 1992 Sep 01; 44(1):18-23. PubMed ID: 1519644
    [Abstract] [Full Text] [Related]

  • 2. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
    Stratton RF, Dobyns WB, Greenberg F, DeSana JB, Moore C, Fidone G, Runge GH, Feldman P, Sekhon GS, Pauli RM.
    Am J Med Genet; 1986 Jul 01; 24(3):421-32. PubMed ID: 3728561
    [Abstract] [Full Text] [Related]

  • 3. Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q.
    Thomas JA, Manchester DK, Prescott KE, Milner R, McGavran L, Cohen MM.
    Am J Med Genet; 1996 Apr 24; 62(4):372-5. PubMed ID: 8723067
    [Abstract] [Full Text] [Related]

  • 4. Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.
    Fryburg JS, Golden WL.
    Am J Med Genet; 1993 Mar 01; 45(5):638-41. PubMed ID: 7681252
    [Abstract] [Full Text] [Related]

  • 5. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
    Liang DS, Wu LQ, Cai F, Xia K, Long ZG, Pan Q, Dai HP, Xia JH.
    Yi Chuan Xue Bao; 2005 Feb 01; 32(2):124-9. PubMed ID: 15759858
    [Abstract] [Full Text] [Related]

  • 6. Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2.
    Aughton DJ, Cassidy SB, Whiteman DA, Delach JA, Guttmacher AE.
    Am J Med Genet; 1991 Sep 15; 40(4):440-3. PubMed ID: 1746608
    [Abstract] [Full Text] [Related]

  • 7. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
    Chitayat D, Ruvalcaba RH, Babul R, Teshima IE, Posnick JC, Vekemans MJ, Scarpelli H, Thuline H.
    Am J Med Genet; 1995 Jan 16; 55(2):147-54. PubMed ID: 7717413
    [Abstract] [Full Text] [Related]

  • 8. [7p-deletion syndrome].
    Hinkel GK, Tolkendorf E, Bergan J.
    Monatsschr Kinderheilkd; 1988 Dec 16; 136(12):824-7. PubMed ID: 3237228
    [Abstract] [Full Text] [Related]

  • 9. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4.
    Beall MH, Falk RE, Ying KL.
    Am J Med Genet; 1988 Nov 16; 31(3):553-7. PubMed ID: 3067576
    [Abstract] [Full Text] [Related]

  • 10. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
    Davies J, Voullaire L, Bankier A.
    Ann Genet; 1990 Nov 16; 33(2):92-5. PubMed ID: 2241091
    [Abstract] [Full Text] [Related]

  • 11. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C, Carvajal MV, Moscatello D, Towner J, Lacassie Y.
    Am J Med Genet; 1995 Mar 13; 56(1):1-5. PubMed ID: 7747769
    [Abstract] [Full Text] [Related]

  • 12. A contiguous gene deletion syndrome at 7q21-q22 and implications for a relationship between isolated ectrodactyly and syndromic ectrodactyly.
    Nunes ME, Pagon RA, Disteche CJ, Evans JP.
    Clin Dysmorphol; 1994 Oct 13; 3(4):277-86. PubMed ID: 7894731
    [Abstract] [Full Text] [Related]

  • 13. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
    Koiffmann CP, Gonzalez CH, Vianna-Morgante AM, Kim CA, Odone-Filho V, Wajntal A.
    Am J Med Genet; 1995 Jul 31; 58(1):46-9. PubMed ID: 7573155
    [Abstract] [Full Text] [Related]

  • 14. Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
    White DM, Pillers DA, Reiss JA, Brown MG, Magenis RE.
    Am J Med Genet; 1995 Jul 17; 57(4):588-97. PubMed ID: 7573135
    [Abstract] [Full Text] [Related]

  • 15. De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
    Redha MA, Krishna Murthy DS, al-Awadi SA, al-Sulaiman IS, Sabry MA, el-Bahey SA, Farag TI.
    Ann Genet; 1996 Jul 17; 39(1):5-9. PubMed ID: 9297445
    [Abstract] [Full Text] [Related]

  • 16. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review.
    Boles RG, Pober BR, Gibson LH, Willis CR, McGrath J, Roberts DJ, Yang-Feng TL.
    Am J Med Genet; 1995 Jan 16; 55(2):155-60. PubMed ID: 7717414
    [Abstract] [Full Text] [Related]

  • 17. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
    Meng J, Fujita H, Nagahara N, Kashiwai A, Yoshioka Y, Funato M.
    Am J Med Genet; 1992 Jul 01; 43(4):747-50. PubMed ID: 1621768
    [Abstract] [Full Text] [Related]

  • 18. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S, Wang S, Hoang K, Vanchiere CM, England K, Fick R, Pagon B, Reddy KS.
    Am J Med Genet; 1999 Nov 05; 87(1):17-22. PubMed ID: 10528241
    [Abstract] [Full Text] [Related]

  • 19. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P, Vögtel D.
    Am J Med Genet; 1987 Oct 05; 28(2):371-6. PubMed ID: 3322005
    [Abstract] [Full Text] [Related]

  • 20. 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]

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