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Journal Abstract Search

157 related items for PubMed ID: 16906570

  • 21. Congenital distal humeral dysplasia: a case report.
    Joseph B, Varghese RA.
    Pediatr Radiol; 2003 Jan; 33(1):7-10. PubMed ID: 12497228
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  • 22. Subtelomeric 6p25 deletion/duplication: Report of a patient with new clinical findings and genotype-phenotype correlations.
    Linhares ND, Svartman M, Rodrigues TC, Rosenberg C, Valadares ER.
    Eur J Med Genet; 2015 May; 58(5):310-8. PubMed ID: 25817395
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  • 26. 6q22.33 microdeletion in a family with intellectual disability, variable major anomalies, and behavioral abnormalities.
    Mackenroth L, Hackmann K, Beyer A, Schallner J, Novotna B, Klink B, Schröck E, Di Donato N.
    Am J Med Genet A; 2015 Nov; 167A(11):2800-7. PubMed ID: 26334553
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  • 31. Poly-epiphyseal overgrowth: description of a previously unreported skeletal dysplasia.
    Pazzaglia UE, Beluffi G, Marchi A, Bozzola M, Savasta S, Bonaspetti G.
    Pediatr Radiol; 2007 Oct; 37(10):1025-30. PubMed ID: 17653707
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  • 33. Dental anomalies in Axenfeld-Rieger syndrome.
    O'Dwyer EM, Jones DC.
    Int J Paediatr Dent; 2005 Nov; 15(6):459-63. PubMed ID: 16238657
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  • 38. Array-CGH and clinical characterization in a patient with subtelomeric 6p deletion without ocular dysgenesis.
    Piccione M, Antona R, Salzano E, Cavani S, Malacarne M, Morreale Bubella R, Pierluigi M, Viaggi CD, Corsello G.
    Am J Med Genet A; 2012 Jan; 158A(1):150-4. PubMed ID: 22105932
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  • 40. A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene.
    Chen CP, Lin SP, Chern SR, Wu PS, Su JW, Wang W.
    Genet Couns; 2013 Jan; 24(2):243-6. PubMed ID: 24032297
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