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Journal Abstract Search

278 related items for PubMed ID: 8741931

  • 21. Broad clinical spectrum in Silver-Russell syndrome and consequences for genetic testing in growth retardation.
    Eggermann T, Gonzalez D, Spengler S, Arslan-Kirchner M, Binder G, Schönherr N.
    Pediatrics; 2009 May; 123(5):e929-31. PubMed ID: 19364767
    [Abstract] [Full Text] [Related]

  • 22. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
    Guttmacher AE.
    Am J Med Genet; 1993 Apr 15; 46(2):219-22. PubMed ID: 8484413
    [Abstract] [Full Text] [Related]

  • 23. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review.
    Bastaki L, El-Nabi MM, Azab AS, Gouda SA, Al-Wadaani AM, Naguib KK.
    East Mediterr Health J; 2007 Apr 15; 13(4):975-9. PubMed ID: 17955782
    [No Abstract] [Full Text] [Related]

  • 24. An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands.
    Preece MA, Abu-Amero SN, Ali Z, Abu-Amero KK, Wakeling EL, Stanier P, Moore GE.
    J Med Genet; 1999 Jun 15; 36(6):457-60. PubMed ID: 10874633
    [Abstract] [Full Text] [Related]

  • 25. Monozygotic twins discordant for the Russell-Silver syndrome.
    Bailey W, Popovich B, Jones KL.
    Am J Med Genet; 1995 Aug 28; 58(2):101-5. PubMed ID: 8533797
    [Abstract] [Full Text] [Related]

  • 26. Brief clinical report: the Dubowitz syndrome in a teenager.
    Fryns JP, Fabry G, Willemyns F, Van Den Berghe H.
    Am J Med Genet; 1979 Aug 28; 4(4):345-7. PubMed ID: 575467
    [Abstract] [Full Text] [Related]

  • 27. Autosomal dominant inheritance of the Aarskog syndrome.
    Grier RE, Farrington FH, Kendig R, Mamunes P.
    Am J Med Genet; 1983 May 28; 15(1):39-46. PubMed ID: 6344635
    [Abstract] [Full Text] [Related]

  • 28. New syndrome: mixed hearing loss, mental deficiency, growth retardation, short clubbed digits, and EEG abnormalities in monozygous female twins.
    Pfeiffer RA.
    Am J Med Genet; 1987 Jul 28; 27(3):639-44. PubMed ID: 3631135
    [No Abstract] [Full Text] [Related]

  • 29. Craniofacial and dental characteristics of Silver-Russell syndrome.
    Kotilainen J, Hölttä P, Mikkonen T, Arte S, Sipilä I, Pirinen S.
    Am J Med Genet; 1995 Mar 27; 56(2):229-36. PubMed ID: 7625451
    [Abstract] [Full Text] [Related]

  • 30. Cataracts, aberrant oral frenula, and growth retardation: a new autosomal dominant syndrome.
    Wellesley D, Carman P, French N, Goldblatt J.
    Am J Med Genet; 1991 Sep 01; 40(3):341-2. PubMed ID: 1951441
    [Abstract] [Full Text] [Related]

  • 31. Craniomicromelic syndrome: a newly recognized lethal condition with craniosynostosis, distinct facial anomalies, short limbs, and intrauterine growth retardation.
    Barr M, Heidelberger KP, Comstock CH.
    Am J Med Genet; 1995 Sep 25; 58(4):348-52. PubMed ID: 8533844
    [Abstract] [Full Text] [Related]

  • 32. [Silver-Russell's syndrome].
    Balslev T, Hansen US.
    Ugeskr Laeger; 1990 Jul 09; 152(28):2053-4. PubMed ID: 2368205
    [Abstract] [Full Text] [Related]

  • 33. Autosomal recessive Silver-Russell syndrome.
    Teebi AS.
    Clin Dysmorphol; 1992 Jul 09; 1(3):151-6. PubMed ID: 1285272
    [Abstract] [Full Text] [Related]

  • 34. Report of a case and further delineation of the SHORT syndrome.
    Toriello HV, Wakefield S, Komar K, Higgins JV, Waterman DF.
    Am J Med Genet; 1985 Oct 09; 22(2):311-4. PubMed ID: 4050863
    [Abstract] [Full Text] [Related]

  • 35. Another case of the autosomal recessive Weaver-like syndrome.
    Slaney SF, Winter RM.
    Am J Med Genet; 1997 Oct 31; 72(3):369-70. PubMed ID: 9332672
    [No Abstract] [Full Text] [Related]

  • 36. A further patient with the Pitt-Rogers-Danks syndrome of mental retardation, unusual face, and intrauterine growth retardation.
    Donnai D.
    Am J Med Genet; 1986 May 31; 24(1):29-32. PubMed ID: 3706410
    [Abstract] [Full Text] [Related]

  • 37. Hepatocellular carcinoma in a child with familial Russell-Silver syndrome.
    Chitayat D, Friedman JM, Anderson L, Dimmick JE.
    Am J Med Genet; 1988 Dec 31; 31(4):909-14. PubMed ID: 2853572
    [Abstract] [Full Text] [Related]

  • 38. Fryns syndrome phenotype and trisomy 22.
    Ladonne JM, Gaillard D, Carré-Pigeon F, Gabriel R.
    Am J Med Genet; 1996 Jan 02; 61(1):68-70. PubMed ID: 8741922
    [Abstract] [Full Text] [Related]

  • 39. Mental retardation, unusual face, and intrauterine growth retardation: a new recessive syndrome?
    Pitt DB, Rogers JG, Danks DM.
    Am J Med Genet; 1984 Oct 02; 19(2):307-13. PubMed ID: 6542309
    [Abstract] [Full Text] [Related]

  • 40. Silver-Russell syndrome and exclusion of uniparental disomy.
    Ayala-Madrigal ML, Shaffer LG, Ramírez-Dueñas ML.
    Clin Genet; 1996 Dec 02; 50(6):494-7. PubMed ID: 9147881
    [Abstract] [Full Text] [Related]

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