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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

290 related items for PubMed ID: 3067576

  • 21. Multiple critical smallest region of overlap in monosomy 16Q syndrome?
    Doco-Fenzy M, Elchardus JF, Brami G, Digeon B, Gruson N, Adnet JJ.
    Genet Couns; 1994; 5(1):39-44. PubMed ID: 8031534
    [Abstract] [Full Text] [Related]

  • 22. Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome.
    Ioan DM, Maximilian C, Kleczkowska A, Fryns JP.
    Ann Genet; 1992; 35(3):167-9. PubMed ID: 1466567
    [Abstract] [Full Text] [Related]

  • 23. A translocation between chromosome 1 and 10 in a boy with mental retardation and dysmorphic features.
    Gambhir PS, Gole LA, Tembe MV, Saraph AA, Phadke MA, Khedkar VA.
    Indian Pediatr; 1991 Mar; 28(3):289-91. PubMed ID: 1937707
    [No Abstract] [Full Text] [Related]

  • 24. Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies.
    Back E, Hertel C, Vogel W, Bettecken F, Thiesen M.
    Ann Genet; 1977 Dec; 20(4):294-6. PubMed ID: 305761
    [Abstract] [Full Text] [Related]

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

  • 26. Interstitial deletion of chromosome 3p: report of a patient and delineation of a proximal 3p deletion syndrome.
    Neri G, Reynolds JF, Westphal J, Hinz J, Daniel A.
    Am J Med Genet; 1984 Sep; 19(1):189-93. PubMed ID: 6496569
    [Abstract] [Full Text] [Related]

  • 27. Deletions of different segments of the long arm of chromosome 4.
    Mitchell JA, Packman S, Loughman WD, Fineman RM, Zackai E, Patil SR, Emanual B, Bartley JA, Hanson JW.
    Am J Med Genet; 1981 Sep; 8(1):73-89. PubMed ID: 7246608
    [Abstract] [Full Text] [Related]

  • 28. Interstitial deletion of long arm of chromosome 13.
    Carnevale A, Frias S, Alcantar R.
    Ann Genet; 1984 Sep; 27(1):49-52. PubMed ID: 6609673
    [Abstract] [Full Text] [Related]

  • 29. Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases.
    Poissonnier M, Turleau C, Olivier-Martin M, Milleret-Proyart MJ, Prieur M, Dubos M, Cabanis MO, Mugneret F, Blanc P, Noel L.
    Ann Genet; 1992 Sep; 35(3):146-51. PubMed ID: 1466563
    [Abstract] [Full Text] [Related]

  • 30. [Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].
    Zaletaev DV, Dadali EL, Kuleshov NP.
    Tsitol Genet; 1987 Sep; 21(3):213-6. PubMed ID: 3617217
    [Abstract] [Full Text] [Related]

  • 31. Novel findings in a patient with Weaver or a Weaver-like syndrome.
    Scarano G, Della Monica M, Lonardo F, Neri G.
    Am J Med Genet; 1996 May 17; 63(2):378-81. PubMed ID: 8725789
    [Abstract] [Full Text] [Related]

  • 32. Proximal interstitial 6q deletion: a recognizable syndrome.
    Kumar R, Riordan D, Dawson AJ, Chudley AE.
    Am J Med Genet; 1997 Aug 22; 71(3):353-6. PubMed ID: 9268108
    [Abstract] [Full Text] [Related]

  • 33. Two infants with del(3)(p25pter) and a review of previously reported cases.
    Ramer JC, Ladda RL, Frankel C.
    Am J Med Genet; 1989 May 22; 33(1):108-12. PubMed ID: 2665488
    [Abstract] [Full Text] [Related]

  • 34. Interstitial deletion of 4(q21q25) in a liveborn male.
    Rose NC, Schneider A, McDonald-McGinn DM, Caserta C, Emanuel BS, Zackai EH.
    Am J Med Genet; 1991 Jul 01; 40(1):77-9. PubMed ID: 1887853
    [Abstract] [Full Text] [Related]

  • 35. 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]

  • 36. Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del (17)(p11.2p11.2).
    Kondo I, Matsuura S, Kuwajima K, Tokashiki M, Izumikawa Y, Naritomi K, Niikawa N, Kajii T.
    Am J Med Genet; 1991 Nov 01; 41(2):225-9. PubMed ID: 1785639
    [Abstract] [Full Text] [Related]

  • 37. 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]

  • 38. Report of two cases of distal deletion of the long arm of chromosome 6.
    Stevens CA, Fineman RM, Breg WR, Silken AB.
    Am J Med Genet; 1988 Apr 30; 29(4):807-14. PubMed ID: 3400725
    [Abstract] [Full Text] [Related]

  • 39. Mirror image duplication of the hands and feet: report of a sporadic case with multiple congenital anomalies.
    Hersh JH, Dela Cruz TV, Pietrantoni M, von Drasek-Ascher G, Turnquest MA, Yacoub OA, Joyce MR.
    Am J Med Genet; 1995 Nov 20; 59(3):341-5. PubMed ID: 8599358
    [Abstract] [Full Text] [Related]

  • 40. A 797 kb de novo deletion of 18q21.31 in a patient with speech delay, mental retardation, sleeping problems, facial dysmorphism, and feet anomalies.
    van Diepen MM, Gijsbers AC, Bosch CA, Oudesluys-Murphy AM, Ruivenkamp CA, Bijlsma EK.
    Eur J Med Genet; 2011 Nov 20; 54(1):86-8. PubMed ID: 20870045
    [Abstract] [Full Text] [Related]

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