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PUBMED FOR HANDHELDS

Journal Abstract Search


134 related items for PubMed ID: 6683959

  • 1. [Robinow's syndrome. Apropos of a case with thrombopenia].
    Khayat D, Schaison G, Frija J, Szpirglas H.
    Arch Fr Pediatr; 1983 Apr; 40(4):327-30. PubMed ID: 6683959
    [Abstract] [Full Text] [Related]

  • 2. [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
    [Abstract] [Full Text] [Related]

  • 3. [Robinow's syndrome].
    Khayat D, Szpirglas H, Lemonnier MP, Laufer J, Schaison G.
    Rev Stomatol Chir Maxillofac; 1983 Dec; 84(4):222-4. PubMed ID: 6579596
    [Abstract] [Full Text] [Related]

  • 4. [Robinow's syndrome with dominant transmission].
    Vallée L, Van Nerom PY, Ferraz FG, Delecour M, Maroteaux P, Farriaux JP, Fontaine G.
    Arch Fr Pediatr; 1982 Dec; 39(7):447-8. PubMed ID: 7149891
    [Abstract] [Full Text] [Related]

  • 5. [Clinical and genetic heterogeneity in Robinow's syndrome. Report of a new case and review of the literature I].
    Oliván Gonzalvo G, Pérez González JM, Ventura Faci P, Olivares López JL, Bueno Sánchez M.
    An Esp Pediatr; 1990 Jul; 33(1):76-81. PubMed ID: 2252296
    [No Abstract] [Full Text] [Related]

  • 6. [Metacarpophalangeal pattern as well as length and proportions of the bones of the extremities in an infant with Robinow's syndrome II].
    Oliván Gonzalvo G, Sarriá Chueca A, Ventura Faci P, Pérez González JM, Bueno Sánchez M.
    An Esp Pediatr; 1990 Jul; 33(1):82-4. PubMed ID: 2252297
    [No Abstract] [Full Text] [Related]

  • 7. [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 Jul; 19(2):121-4. PubMed ID: 9312747
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Robinow syndrome.
    Singh SK, Bhadada SK, Singh R, Sinha SK, Singh SK, Agrawal JK.
    J Assoc Physicians India; 2000 Aug; 48(8):836-7. PubMed ID: 11273483
    [Abstract] [Full Text] [Related]

  • 10. [Robinow syndrome (fetal-face dwarfism). Presentation of a case and review of the literature].
    Rodríguez Costa T, García De León R, Casas Fernández C, Puche Mira A, Pérez Bryan J.
    An Esp Pediatr; 1984 Jan; 20(1):55-61. PubMed ID: 6703533
    [Abstract] [Full Text] [Related]

  • 11. Is the frequency of Robinow syndrome relatively high in Turkey? Four more case reports.
    Akşit S, Aydinlioglu H, Dizdarer G, Caglayan S, Bektaşlar D, Cin A.
    Clin Genet; 1997 Oct; 52(4):226-30. PubMed ID: 9383028
    [Abstract] [Full Text] [Related]

  • 12. Robinow Syndrome: a case report.
    Gulcan H, Akinci A, Aktar A.
    Genet Couns; 2005 Oct; 16(3):297-300. PubMed ID: 16259327
    [Abstract] [Full Text] [Related]

  • 13. [Duplication of mouth and mandible. Apropos of a case].
    Chaouachi B, Ben Salah S, Trabelsi M, Maherzi A, Lakhoua R.
    Ann Pediatr (Paris); 1990 Mar; 37(3):193-4. PubMed ID: 2350148
    [Abstract] [Full Text] [Related]

  • 14. [Anesthesia and fibrobronchoscopy for the study of chronic stridor in a boy with Robinow syndrome].
    Cassinello Ogea C, Gil Berduque L, Oliva Perales P, Casado Merodio AI, Izquierdo Villarrolla B, Fernández Liesa JI.
    Rev Esp Anestesiol Reanim; 2003 Feb; 50(2):101-5. PubMed ID: 12712873
    [Abstract] [Full Text] [Related]

  • 15. Sclerocornea, hypertelorism, syndactyly, and ambiguous genitalia.
    Martínez-Frías ML, Bermejo E, Sánchez Otero T, Urioste M, Morena V, Cruz E.
    Am J Med Genet; 1994 Jan 15; 49(2):195-7. PubMed ID: 8116666
    [Abstract] [Full Text] [Related]

  • 16. Dup(1q)(q42-->qter) syndrome: case report and review of literature.
    Kennerknecht I, Barbi G, Rodens K.
    Am J Med Genet; 1993 Dec 01; 47(8):1157-60. PubMed ID: 7507296
    [Abstract] [Full Text] [Related]

  • 17. Robinow syndrome.
    Bhandari B, Tak SK, Gupta RS, Ramakrishnan S.
    Indian Pediatr; 1988 Aug 01; 25(8):784-6. PubMed ID: 3220568
    [No Abstract] [Full Text] [Related]

  • 18. [Robinow's fetal face-dwarfism syndrome].
    Seel RE, Wörner I, Passarge E.
    Monatsschr Kinderheilkd (1902); 1974 Jul 01; 122(7):663-4. PubMed ID: 4410798
    [No Abstract] [Full Text] [Related]

  • 19. [Intrauterine dwarfism and dysmorfic features. A case of Russel-Silver syndrome].
    Peinado Garrido A, Borja Pérez C, Narbona López E, Contreras Chova F, Jerez Calero A, Miras Baldó M.
    An Esp Pediatr; 2001 Jun 01; 54(6):588-90. PubMed ID: 11412408
    [Abstract] [Full Text] [Related]

  • 20. Teebi hypertelorism syndrome: further observations.
    Tsukahara M, Uchida M, Shinohara T.
    Am J Med Genet; 1995 Oct 23; 59(1):59-61. PubMed ID: 8849013
    [Abstract] [Full Text] [Related]


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