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PUBMED FOR HANDHELDS

Journal Abstract Search

178 related items for PubMed ID: 4019538

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  • 2. [Tarsal-carpal coalition syndrome: a familial case].
    Caino S, Dello Ruso B, Fano V, Obregón MG.
    An Pediatr (Barc); 2012 Jun; 76(6):355-9. PubMed ID: 22326510
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  • 4. Symphalangism with metacarpophalangeal fusions and elbow abnormalities.
    Kassner EG, Katz I, Qazi QH.
    Pediatr Radiol; 1976 Feb 13; 4(2):103-7. PubMed ID: 967566
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  • 6. Tarsal-carpal coalition syndrome: Report of a novel missense mutation in NOG gene and phenotypic delineation.
    Das Bhowmik A, Salem Ramakumaran V, Dalal A.
    Am J Med Genet A; 2018 Jan 13; 176(1):219-224. PubMed ID: 29159868
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  • 11. Multiple synostosis syndrome: study of a large Brazilian kindred.
    da-Silva EO, Filho SM, de Albuquerque SC.
    Am J Med Genet; 1984 Jun 13; 18(2):237-47. PubMed ID: 6465200
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  • 12. Genetic nosology and counseling of humeroradial synostosis.
    Pfeiffer RA, Braun-Quentin C.
    Genet Couns; 1994 Jun 13; 5(3):269-74. PubMed ID: 7811427
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  • 13. [A complex symphalangia syndrome with brachydactyly, humeroradial synostosis and other multiple joint dysplasias].
    Schumacher KA, Wolf M, Friedrich JM.
    Rontgenblatter; 1988 May 13; 41(5):211-4. PubMed ID: 3393818
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  • 18. Further delineation of facioaudiosymphalangism syndrome: Description of a family with a novel NOG mutation and without hearing loss.
    Bayat A, Fijalkowski I, Andersen T, Abdulmunem SA, van den Ende J, Van Hul W.
    Am J Med Genet A; 2016 Jun 13; 170(6):1479-84. PubMed ID: 26994744
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  • 19. A comprehensive review of reported heritable noggin-associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term: NOG-related-symphalangism spectrum disorder (NOG-SSD).
    Potti TA, Petty EM, Lesperance MM.
    Hum Mutat; 2011 Aug 13; 32(8):877-86. PubMed ID: 21538686
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