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Journal Abstract Search

186 related items for PubMed ID: 9056548

  • 1. Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed.
    Tahseen K, Khan S, Uma R, Usha R, Al Ghanem MM, Al Awadi SA, Farag TI.
    Am J Med Genet; 1997 Mar 17; 69(2):126-32. PubMed ID: 9056548
    [Abstract] [Full Text] [Related]

  • 2. Kenny-Caffey syndrome: an Arab variant?
    Sabry MA, Farag TI, Shaltout AA, Zaki M, Al-Mazidi Z, Abulhassan SJ, Al-Torki N, Quishawi A, Al Awadi SA.
    Clin Genet; 1999 Jan 17; 55(1):44-9. PubMed ID: 10066031
    [Abstract] [Full Text] [Related]

  • 3. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
    Franceschini P, Testa A, Bogetti G, Girardo E, Guala A, Lopez-Bell G, Buzio G, Ferrario E, Piccato E.
    Am J Med Genet; 1992 Jan 01; 42(1):112-6. PubMed ID: 1308349
    [Abstract] [Full Text] [Related]

  • 4. Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster.
    Sabry MA, Zaki M, Abul Hassan SJ, Ramadan DG, Abdel Rasool MA, al Awadi SA, al Saleh Q.
    J Med Genet; 1998 Jan 01; 35(1):31-6. PubMed ID: 9475091
    [Abstract] [Full Text] [Related]

  • 5. Gómez-López-Hernández syndrome in a child born to consanguineous parents: new evidence for an autosomal-recessive pattern of inheritance?
    de Mattos VF, Graziadio C, Machado Rosa RF, Lenhardt R, Alves RP, Trevisan P, Paskulin GA, Zen PR.
    Pediatr Neurol; 2014 Jun 01; 50(6):612-5. PubMed ID: 24690526
    [Abstract] [Full Text] [Related]

  • 6. Oto-facio-osseous-gonadal syndrome: a new form of syndromic deafness?
    da-Silva EO, Duarte AR, Lins TS.
    Clin Genet; 1997 Jul 01; 52(1):51-5. PubMed ID: 9272713
    [Abstract] [Full Text] [Related]

  • 7. Kenny-Caffey syndrome. Case report and literature review.
    Abdel-Al YK, Auger LT, el-Gharbawy F.
    Clin Pediatr (Phila); 1989 Apr 01; 28(4):175-9. PubMed ID: 2649298
    [Abstract] [Full Text] [Related]

  • 8. Sanjad-Sakati syndrome/Kenny-Caffey syndrome type 1: a study of 21 cases in Kuwait.
    Naguib KK, Gouda SA, Elshafey A, Mohammed F, Bastaki L, Azab AS, Alawadi SA.
    East Mediterr Health J; 2009 Apr 01; 15(2):345-52. PubMed ID: 19554981
    [Abstract] [Full Text] [Related]

  • 9. Desbuquois syndrome in an Arab Bedouin family.
    al-Gazeli LI, Aziz SA, Bakalinova D.
    Clin Genet; 1996 Oct 01; 50(4):255-9. PubMed ID: 9001812
    [Abstract] [Full Text] [Related]

  • 10. Cortical blindness, growth and psychomotor retardation and postaxial polydactyly: a probably distinct autosomal recessive syndrome.
    Hernández A, García-Esquivel L, Reynoso MC, Fragoso R, Enríquez-Guerra MA, Nazará Z, Anzar MB, Cantú JM.
    Clin Genet; 1985 Sep 01; 28(3):251-4. PubMed ID: 4064363
    [Abstract] [Full Text] [Related]

  • 11. The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43.
    Diaz GA, Khan KT, Gelb BD.
    Genomics; 1998 Nov 15; 54(1):13-8. PubMed ID: 9806825
    [Abstract] [Full Text] [Related]

  • 12. A radiological and genetic investigation of acheiropody in a kindred including six cases.
    Toledo SP, Saldanha PH.
    J Genet Hum; 1969 May 15; 17(1):81-94. PubMed ID: 5808544
    [No Abstract] [Full Text] [Related]

  • 13. A new autosomal recessive disorder resembling Weaver syndrome.
    Teebi AS, Sundareshan TS, Hammouri MY, al-Awadi SA, al-Saleh QA.
    Am J Med Genet; 1989 Aug 15; 33(4):479-82. PubMed ID: 2596508
    [Abstract] [Full Text] [Related]

  • 14. Autosomal recessive Robinow syndrome.
    Teebi AS.
    Am J Med Genet; 1990 Jan 15; 35(1):64-8. PubMed ID: 2301471
    [Abstract] [Full Text] [Related]

  • 15. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
    [Abstract] [Full Text] [Related]

  • 16. New autosomal recessive multiple congenital abnormalities/mental retardation syndrome with craniofacial dysmorphism absent corpus callosum, iris colobomas and connective tissue dysplasia.
    Temtamy SA, Salam MA, Aboul-Ezz EH, Hussein HA, Helmy SA, Shalash BA.
    Clin Dysmorphol; 1996 Jul 01; 5(3):231-40. PubMed ID: 8818452
    [Abstract] [Full Text] [Related]

  • 17. Autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance.
    al-Gazali LI, Bakalinova D.
    Clin Dysmorphol; 1998 Jul 01; 7(3):177-84. PubMed ID: 9689990
    [Abstract] [Full Text] [Related]

  • 18. Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.
    Temtamy SA, Shoukry AS, Raafat M, Mihareb S.
    Birth Defects Orig Artic Ser; 1975 Jul 01; 11(2):104-8. PubMed ID: 1227520
    [Abstract] [Full Text] [Related]

  • 19. The Meier-Gorlin syndrome, or ear-patella-short stature syndrome, in sibs.
    Loeys BL, Lemmerling MM, Van Mol CE, Leroy JG.
    Am J Med Genet; 1999 May 07; 84(1):61-7. PubMed ID: 10213048
    [Abstract] [Full Text] [Related]

  • 20. [Kenny-Caffey syndrome and its related syndromes].
    Isojima T, Kitanaka S.
    Nihon Rinsho; 2015 Nov 07; 73(11):1959-64. PubMed ID: 26619675
    [Abstract] [Full Text] [Related]

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