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

Journal Abstract Search


675 related items for PubMed ID: 11483842

  • 1. Syndromic ear anomalies and renal ultrasounds.
    Wang RY, Earl DL, Ruder RO, Graham JM.
    Pediatrics; 2001 Aug; 108(2):E32. PubMed ID: 11483842
    [Abstract] [Full Text] [Related]

  • 2. Association of preauricular sinuses and renal anomalies.
    Leung AK, Robson WL.
    Urology; 1992 Sep; 40(3):259-61. PubMed ID: 1523751
    [Abstract] [Full Text] [Related]

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

  • 4. Renal ultrasonography not required in babies with isolated minor ear anomalies.
    Deshpande SA, Watson H.
    Arch Dis Child Fetal Neonatal Ed; 2006 Jan; 91(1):F29-30. PubMed ID: 16223753
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Branchio-oto-renal syndrome.
    Garg A, Wadhera R, Gulati SP, Kumar A.
    J Assoc Physicians India; 2008 Nov; 56():904-5. PubMed ID: 19263692
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Genetic aspects of the BOR syndrome--branchial fistulas, ear pits, hearing loss, and renal anomalies.
    Fraser FC, Ling D, Clogg D, Nogrady B.
    Am J Med Genet; 1978 Nov; 2(3):241-52. PubMed ID: 263442
    [Abstract] [Full Text] [Related]

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

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

  • 12. Congenital conductive or mixed deafness, preauricular sinus, external ear anomaly, and commissural lip pits: an autosomal dominant inherited syndrome.
    Marres HA, Cremers CW.
    Ann Otol Rhinol Laryngol; 1991 Nov; 100(11):928-32. PubMed ID: 1746829
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Hemifacial microsomia and the branchio-oto-renal syndrome.
    Rollnick BR, Kaye CI.
    J Craniofac Genet Dev Biol Suppl; 1985 Nov; 1():287-95. PubMed ID: 3877103
    [Abstract] [Full Text] [Related]

  • 15. Delineation of EFTUD2 haploinsufficiency-related phenotypes through a series of 36 patients.
    Lehalle D, Gordon CT, Oufadem M, Goudefroye G, Boutaud L, Alessandri JL, Baena N, Baujat G, Baumann C, Boute-Benejean O, Caumes R, Decaestecker C, Gaillard D, Goldenberg A, Gonzales M, Holder-Espinasse M, Jacquemont ML, Lacombe D, Manouvrier-Hanu S, Marlin S, Mathieu-Dramard M, Morin G, Pasquier L, Petit F, Rio M, Smigiel R, Thauvin-Robinet C, Vasiljevic A, Verloes A, Malan V, Munnich A, de Pontual L, Vekemans M, Lyonnet S, Attié-Bitach T, Amiel J.
    Hum Mutat; 2014 Apr; 35(4):478-85. PubMed ID: 24470203
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 34.