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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

196 related items for PubMed ID: 9272713

  • 1. Oto-facio-osseous-gonadal syndrome: a new form of syndromic deafness?
    da-Silva EO, Duarte AR, Lins TS.
    Clin Genet; 1997 Jul; 52(1):51-5. PubMed ID: 9272713
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  • 2. 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; 50(6):612-5. PubMed ID: 24690526
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  • 5. Craniometadiaphyseal dysplasia, wormian bone type.
    Santolaya JM, Hall CM, García-Miñaur S, Delgado A.
    Am J Med Genet; 1998 May 18; 77(3):241-5. PubMed ID: 9605592
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  • 8. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A, Young-Wee T, Frye T.
    Am J Med Genet; 1983 May 18; 15(1):71-7. PubMed ID: 6859126
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  • 10. 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
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  • 13. Fronto-facio-nasal dysplasia.
    Suthers G, David D, Clark B.
    Clin Dysmorphol; 1997 Jul 07; 6(3):245-9. PubMed ID: 9220195
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  • 14. Joint laxity, vitreoretinal degeneration, facial abnormalities, and generalized skeletal alterations: a new syndrome?
    Nishimura G, Hasegawa T, Sugii K, Tsuyama K, Matsuo N.
    J Hum Genet; 1998 Jul 07; 43(3):191-4. PubMed ID: 9747034
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  • 15. SAMS: provisionally unique multiple congenital anomalies syndrome consisting of short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities.
    Lemire EG, Hildes-Ripstein GE, Reed MH, Chudley AE.
    Am J Med Genet; 1998 Jan 23; 75(3):256-60. PubMed ID: 9475592
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  • 18. A new syndrome: multiple congenital abnormalities and mental retardation in two brothers.
    Dundar M, Ozdemir SY, Fryns JP.
    Genet Couns; 2012 Jan 23; 23(1):13-8. PubMed ID: 22611637
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  • 19. Two brothers with characteristic facial appearance, severe psychomotor retardation, hypospadias, contractures, and other symptoms: a new recessive syndrome?
    Wolff G, Zimmermann E, Zimmerhackl B, Harnasch C, Jung C, Back E.
    J Med Genet; 1994 Jan 23; 31(1):65-7. PubMed ID: 8151642
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  • 20. An autosomal recessive disorder with retardation of growth, mental deficiency, ptosis, pectus excavatum and camptodactyly.
    Khaldi F, Bennaceur B, Hammou A, Hamza M, Gharbi HA.
    Pediatr Radiol; 1988 Jan 23; 18(5):432-5. PubMed ID: 3174286
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