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Journal Abstract Search

122 related items for PubMed ID: 2649298

  • 1. Kenny-Caffey syndrome. Case report and literature review.
    Abdel-Al YK, Auger LT, el-Gharbawy F.
    Clin Pediatr (Phila); 1989 Apr; 28(4):175-9. PubMed ID: 2649298
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  • 2. Kenny-Caffey syndrome type 1 in an Egyptian girl.
    Metwalley KA, Farghaly HS.
    Indian J Endocrinol Metab; 2012 Sep; 16(5):827-9. PubMed ID: 23087875
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  • 3. Kenny-Caffe syndrome.
    Churesigaew S.
    J Med Assoc Thai; 1994 Oct; 77(10):554-9. PubMed ID: 7745379
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  • 4. 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
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  • 5. 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
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  • 6. The Kenny-Caffey syndrome: growth retardation and hypocalcemia in a young boy.
    Lee WK, Vargas A, Barnes J, Root AW.
    Am J Med Genet; 1983 Apr 17; 14(4):773-82. PubMed ID: 6342392
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  • 9. Further delineation of phenotype and genotype of Kenny-Caffey syndrome type 2 (phenotype and genotype of KCS type 2).
    Chen X, Zou C.
    Mol Genet Genomic Med; 2024 Apr 17; 12(4):e2433. PubMed ID: 38591167
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  • 10. Kenny syndrome: case report and literature review.
    Tsai CE, Chiu PC, Lee ML.
    J Formos Med Assoc; 1996 Oct 17; 95(10):793-7. PubMed ID: 8961678
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  • 11. 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 17; 35(1):31-6. PubMed ID: 9475091
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  • 12. 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
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  • 13. A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2.
    Isojima T, Doi K, Mitsui J, Oda Y, Tokuhiro E, Yasoda A, Yorifuji T, Horikawa R, Yoshimura J, Ishiura H, Morishita S, Tsuji S, Kitanaka S.
    J Bone Miner Res; 2014 Apr 01; 29(4):992-8. PubMed ID: 23996431
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  • 14. Mother and daughter with Kenny-Caffey syndrome: the adult phenotype.
    Tonelli L, Sanchini M, Margutti A, Buldrini B, Superti-Furga A, Ferlini A, Selvatici R, Bigoni S.
    Eur J Med Genet; 2024 Jun 01; 69():104943. PubMed ID: 38679371
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  • 15. Congenital medullary tubular stenosis. A case of Caffey-Kenny syndrome.
    Enriquez EJ, Toledo F, Bustamante-Cruz M, Cruz GM.
    Acta Orthop Scand; 1988 Jun 01; 59(3):326-7. PubMed ID: 3381667
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  • 17. [Arabian variant of Kenny syndrome: a familial case in Tunisia].
    Fitouri Z, Fayech C, Ferchichi M, Ben Becher S.
    Ann Endocrinol (Paris); 2005 Sep 01; 66(4):361-4. PubMed ID: 16392187
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  • 18. Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2.
    Deconte D, Kreusch TC, Salvaro BP, Perin WF, Ferreira MAT, Kopacek C, da Rosa EB, Heringer JI, Ligabue-Braun R, Zen PRG, Rosa RFM, Fiegenbaum M.
    J Pediatr Genet; 2020 Dec 01; 9(4):263-269. PubMed ID: 32765931
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