These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

800 related items for PubMed ID: 17574621

  • 1. Genitourinary anomalies of pediatric FG syndrome.
    Smith JF, Wayment RO, Cartwright PC, Snow BW, Opitz JM.
    J Urol; 2007 Aug; 178(2):656-9. PubMed ID: 17574621
    [Abstract] [Full Text] [Related]

  • 2. Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.
    Lyons MJ, Graham JM, Neri G, Hunter AG, Clark RD, Rogers RC, Moscarda M, Boccuto L, Simensen R, Dodd J, Robertson S, DuPont BR, Friez MJ, Schwartz CE, Stevenson RE.
    J Med Genet; 2009 Jan; 46(1):9-13. PubMed ID: 18805826
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Developmental anomalies and disabilities associated with hypospadias.
    Wu WH, Chuang JH, Ting YC, Lee SY, Hsieh CS.
    J Urol; 2002 Jul; 168(1):229-32. PubMed ID: 12050549
    [Abstract] [Full Text] [Related]

  • 5. Kabuki syndrome and trisomy 10p.
    Utine GE, Alanay Y, Atkaş D, Boduroğlu K, Alikaşifoğlu M, Tunçbilek E.
    Genet Couns; 2008 Jul; 19(3):291-300. PubMed ID: 18990985
    [Abstract] [Full Text] [Related]

  • 6. A clinical study of Sotos syndrome patients with review of the literature.
    Leventopoulos G, Kitsiou-Tzeli S, Kritikos K, Psoni S, Mavrou A, Kanavakis E, Fryssira H.
    Pediatr Neurol; 2009 May; 40(5):357-64. PubMed ID: 19380072
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome.
    Risheg H, Graham JM, Clark RD, Rogers RC, Opitz JM, Moeschler JB, Peiffer AP, May M, Joseph SM, Jones JR, Stevenson RE, Schwartz CE, Friez MJ.
    Nat Genet; 2007 Apr; 39(4):451-3. PubMed ID: 17334363
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Scoliosis in velo-cardio-facial syndrome.
    Morava E, Lacassie Y, King A, Illes T, Marble M.
    J Pediatr Orthop; 2002 Apr; 22(6):780-3. PubMed ID: 12409907
    [Abstract] [Full Text] [Related]

  • 14. The FG syndrome: further characterization, report of a third family, and of a sporadic case.
    Riccardi VM, Hässler E, Lubinsky MS.
    Am J Med Genet; 1977 Apr; 1(1):47-58. PubMed ID: 565138
    [Abstract] [Full Text] [Related]

  • 15. [Congenital malformations of the genitourinary tract in children with Smith-Lemli-Opitz syndrome].
    Wolski JK, Krajewska-Walasek M, Szymkiewicz C.
    Wiad Lek; 1998 Apr; 51 Suppl 3():129-33. PubMed ID: 9814122
    [Abstract] [Full Text] [Related]

  • 16. Craniosynostosis in Kabuki syndrome.
    Martínez-Lage JF, Felipe-Murcia M, Navarro EG, Almagro MJ, López-Guerrero AL, Pérez-Espejo MA.
    J Neurosurg Pediatr; 2010 Aug; 6(2):198-201. PubMed ID: 20672944
    [Abstract] [Full Text] [Related]

  • 17. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L, Hellin AC, Jamar M, Pierquin G, Bours V, Verloes A.
    Genet Couns; 2007 Aug; 18(2):201-7. PubMed ID: 17710872
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Distinct familial syndrome of severe to profound mental retardation, spastic paraplegia with contrasting axial hypotonia, short stature and distinct craniofacial appearance with nasal hypoplasia.
    Fryns JP, Devriendt K, Detroch C, Decock P.
    Genet Couns; 1998 Aug; 9(1):51-4. PubMed ID: 9555588
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 40.