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PUBMED FOR HANDHELDS

Journal Abstract Search

137 related items for PubMed ID: 2679089

  • 1. Apparent Ruvalcaba syndrome with genitourinary abnormalities.
    Bialer MG, Wilson WG, Kelly TE.
    Am J Med Genet; 1989 Jul; 33(3):314-7. PubMed ID: 2679089
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  • 3. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
    Brooks SS, Wisniewski K, Brown WT.
    Am J Med Genet; 1994 Jul 15; 51(4):586-90. PubMed ID: 7943044
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  • 5. A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome.
    Bottani A, Schinzel A.
    Clin Dysmorphol; 1993 Jul 15; 2(3):225-31. PubMed ID: 8287184
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  • 7. Genitourinary anomalies of pediatric FG syndrome.
    Smith JF, Wayment RO, Cartwright PC, Snow BW, Opitz JM.
    J Urol; 2007 Aug 15; 178(2):656-9. PubMed ID: 17574621
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  • 8. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
    Tsukahara M, Sugio Y.
    J Hum Genet; 1998 Aug 15; 43(4):224-7. PubMed ID: 9852671
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  • 9. New syndrome?: MCA/MR syndrome with multiple circumferential skin creases.
    Elliott AM, Ludman M, Teebi AS.
    Am J Med Genet; 1996 Mar 01; 62(1):23-5. PubMed ID: 8779319
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  • 11. Cerebro-osseous-digital syndrome: four new cases of a lethal skeletal dysplasia--distinct from Neu-Laxova Syndrome.
    Elliott AM, Gonzales M, Hoeffel JC, Le Merrer M, Maroteaux P, Encha-Razavi F, Joye N, Berchel C, Fliegel C, Aughton DJ, Beaudry-Rodgers K, Hasteh F, Nerlich AG, Wilcox WR, Rimoin DL, Lachman RS, Freisinger P.
    Am J Med Genet; 2002 Apr 22; 109(2):139-48. PubMed ID: 11977163
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  • 12. Aarskog syndrome: report of a family with review and discussion of nosology.
    Teebi AS, Rucquoi JK, Meyn MS.
    Am J Med Genet; 1993 Jun 15; 46(5):501-9. PubMed ID: 8322809
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  • 13. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.
    Feingold M, Hall BD, Lacassie Y, Martínez-Frías ML.
    Am J Med Genet; 1997 Mar 31; 69(3):245-9. PubMed ID: 9096752
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  • 15. Kabuki make-up syndrome with unilateral renal agenesis.
    Rosti RO, Kayserili H.
    Turk J Pediatr; 2009 Mar 31; 51(3):298-300. PubMed ID: 19817278
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  • 16. [About "a new syndrome" associated with a familial translocation 13/14 (author's transl)].
    Geormaneanu M, Bene M, Geormaneanu C, Walter A.
    Klin Padiatr; 1978 Sep 31; 190(5):500-6. PubMed ID: 568201
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  • 18. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG, Reed SD, Rosenbaum KN, Gershanik J, Chen H, Wilson KM.
    Am J Med Genet; 1982 Aug 31; 12(4):377-409. PubMed ID: 7124793
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  • 19. Ohdo-like blepharophimosis syndrome with distinctive facies, neonatal hypotonia, mental retardation and hypoplastic teeth.
    Clayton-Smith J, Krajewska-Walasek M, Fryer A, Donnai D.
    Clin Dysmorphol; 1994 Apr 31; 3(2):115-20. PubMed ID: 8055130
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  • 20. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC.
    Pediatrics; 2008 Feb 31; 121(2):404-10. PubMed ID: 18245432
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