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Journal Abstract Search

164 related items for PubMed ID: 3688772

  • 1. [A syndrome of mandibulofacial dysostosis associated with a chromosome anomaly].
    Chabrolle JP, Chauveau P, Le Luyer B, Delaporte B, Coudray J.
    Ann Pediatr (Paris); 1987 Oct; 34(8):641-3. PubMed ID: 3688772
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  • 3. Trisomy 9 mosaicism: another etiology for the manifestations of Goldenhar syndrome.
    Wilson GN, Barr M.
    J Craniofac Genet Dev Biol; 1983 Oct; 3(4):313-6. PubMed ID: 6662905
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  • 4. Differential diagnosis of Nager acrofacial dysostosis syndrome: report of four patients with Nager syndrome and discussion of other related syndromes.
    Halal F, Herrmann J, Pallister PD, Opitz JM, Desgranges MF, Grenier G.
    Am J Med Genet; 1983 Feb; 14(2):209-24. PubMed ID: 6837625
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  • 6. Mild mandibulofacial dysostosis in a child with a deletion of 3p.
    Arn PH, Mankinen C, Jabs EW.
    Am J Med Genet; 1993 Jun 15; 46(5):534-6. PubMed ID: 8322816
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  • 7. Terminal deletion 6q syndrome with 11q partial trisomy mosaicism due to maternal balanced translocation.
    Imataka G, Okuya M, Hirao J, Arisaka O.
    Genet Couns; 2014 Jun 15; 25(1):63-7. PubMed ID: 24783657
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  • 8. Sporadic, idiopathic MCA syndrome with mandibulofacial dysostosis and tibial hemimelia.
    Richieri-Costa A, Guion-Almeida ML, van den Ende J.
    Am J Med Genet; 1991 Dec 01; 41(3):330-2. PubMed ID: 1789289
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  • 11. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].
    Stankiewicz P, Korniszewski L, Bocian E, Stańczak H.
    Pediatr Pol; 1996 Mar 01; 71(3):241-5. PubMed ID: 8966096
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  • 12. [A genetic study and clinical classification of 154 cases of mandibulofacial dystosis (Franceschetti's syndrome), with descriptions of associated malformations].
    Vatré JL.
    J Genet Hum; 1971 Mar 01; 19(1):17-100. PubMed ID: 5003458
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  • 13. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
    Urioste M, Visedo G, Sanchís A, Sentís C, Villa A, Ludeña P, Hortigüela JL, Martínez-Frías ML, Fernández-Piqueras J.
    Am J Med Genet; 1994 Jan 01; 49(1):77-82. PubMed ID: 8172255
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  • 19. Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.
    Kobrynski L, Chitayat D, Zahed L, McGregor D, Rochon L, Brownstein S, Vekemans M, Albert DL.
    Am J Med Genet; 1993 Apr 01; 46(1):68-71. PubMed ID: 8494034
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