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Journal Abstract Search

162 related items for PubMed ID: 8053771

  • 1. [Robinow's syndrome associated with deafness].
    Samoud A, Menif K, Boulaares M, Ben Dridi MF.
    Arch Fr Pediatr; 1993 Dec; 50(10):897-9. PubMed ID: 8053771
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  • 2. Robinow Syndrome: a case report.
    Gulcan H, Akinci A, Aktar A.
    Genet Couns; 2005 Dec; 16(3):297-300. PubMed ID: 16259327
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  • 4. Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient.
    Cerqueira DF, de Souza IP.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Mar; 105(3):353-7. PubMed ID: 18061493
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  • 8. Acrocallosal syndrome in two African brothers born to consanguineous parents.
    Christianson AL, Venter PA, Du Toit JL, Shipalana N, Gericke GS.
    Am J Med Genet; 1994 Jun 01; 51(2):98-101. PubMed ID: 8092201
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  • 9. [Cryptorchidism with didymo-epididymal dissociation and Robinow's syndrome: 2 case reports].
    Fabbro MA, D'Agostino S, Costa L, Musi L, Cappellari F.
    Pediatr Med Chir; 1997 Jun 01; 19(2):121-4. PubMed ID: 9312747
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  • 10. Mild optic nerve hypoplasia with retinal venous tortuosity in aarskog (facial-digital-genital) syndrome.
    Jogiya A, Sandy C.
    Ophthalmic Genet; 2005 Sep 01; 26(3):139-41. PubMed ID: 16272060
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  • 11. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A, Young-Wee T, Frye T.
    Am J Med Genet; 1983 May 01; 15(1):71-7. PubMed ID: 6859126
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  • 13. Oto-palato-digital syndrome type II.
    Stoll C, Alembik Y.
    Genet Couns; 1994 May 01; 5(1):61-6. PubMed ID: 8031537
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  • 14. [Robinow's syndrome in a family of consanguineous marriages].
    Gómez-Valencia L, Nájera-Martínez P.
    Bol Med Hosp Infant Mex; 1989 Apr 01; 46(4):303-4. PubMed ID: 2719815
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  • 16. Familial occurrence of renal and Müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay.
    Davee MA, Moore CA, Bull MJ, Hodes ME.
    Am J Med Genet; 1992 Oct 01; 44(3):293-6. PubMed ID: 1283287
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  • 19. Concurrence of Robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins.
    Nazer H, Gunasekaran TS, Sakati NA, Nyhan WL.
    Am J Med Genet; 1990 Dec 01; 37(4):516-8. PubMed ID: 2260598
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  • 20. Teebi hypertelorism syndrome: report of a third family.
    Toriello HV, Delp K.
    Clin Dysmorphol; 1994 Oct 01; 3(4):335-9. PubMed ID: 7894738
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