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Journal Abstract Search

544 related items for PubMed ID: 4469994

  • 81. Neonatal hyperthyroidism with accelerated skeletal maturation, craniosynostosis, and brachydactyly.
    Riggs W, Wilroy RS, Etteldorf JN.
    Radiology; 1972 Dec; 105(3):621-5. PubMed ID: 4642468
    [No Abstract] [Full Text] [Related]

  • 82. A case report of brachydactyly types D and E: a new variation of brachydactyly.
    Ridgeway S, Tai CC, Singh D.
    Foot Ankle Int; 2004 Jun; 25(6):419-22. PubMed ID: 15215028
    [No Abstract] [Full Text] [Related]

  • 83. The radiology of Coffin-Lowry syndrome.
    Padley S, Hodgson SV, Sherwood T.
    Br J Radiol; 1990 Jan; 63(745):72-5. PubMed ID: 2306591
    [No Abstract] [Full Text] [Related]

  • 84. Pfeiffer syndrome. An unusual type of acrocephalosyndactyly with broad thumbs and great toes.
    Martsolf JT, Cracco JB, Carpenter GG, O'Hara AE.
    Am J Dis Child; 1971 Mar; 121(3):257-62. PubMed ID: 5551881
    [No Abstract] [Full Text] [Related]

  • 85. Proteus syndrome.
    Samlaska CP, Levin SW, James WD, Benson PM, Walker JC, Perlik PC.
    Arch Dermatol; 1989 Aug; 125(8):1109-14. PubMed ID: 2667470
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  • 86. Proximal symphalangism of fingers associated with fusion of os naviculare and talus and occurrence of two accessory bones in the feet (os paranaviculare and os tibiale externum) in an European--Indonesian--Chinese family.
    Wildervanck LS, Goedhard G, Meijer S.
    Acta Genet Stat Med; 1967 Aug; 17(1):166-77. PubMed ID: 5633139
    [No Abstract] [Full Text] [Related]

  • 87. Dermatoglyphics in patients with Cenani-Lenz type syndactyly: studies in a new case.
    Elçioglu N, Atasu M, Cenani A.
    Am J Med Genet; 1997 Jun 27; 70(4):341-5. PubMed ID: 9182770
    [Abstract] [Full Text] [Related]

  • 88. Conductive deafness, symphalangism, and facial abnormalities: the WL syndrome in a Japanese family.
    Higashi K, Inoue S.
    Am J Med Genet; 1983 Sep 27; 16(1):105-9. PubMed ID: 6638061
    [Abstract] [Full Text] [Related]

  • 89. Anomalies of the fingers and toes associated with Klippel-Trenaunay syndrome.
    McGrory BJ, Amadio PC, Dobyns JH, Stickler GB, Unni KK.
    J Bone Joint Surg Am; 1991 Dec 27; 73(10):1537-46. PubMed ID: 1660897
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  • 93. A new form of spondyloperipheral dysplasia with facial dysmorphism, flattened vertebrae, hypoplastic pelvis, brachydactyly and soft tissue syndactyly.
    Kitoh H, Lachman RS.
    Pediatr Radiol; 2001 Jan 27; 31(1):23-6. PubMed ID: 11200993
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  • 98. Familial pachydermoperiostosis presenting as an acromegaly-like syndrome.
    Harbison JB, Nice CM.
    Am J Roentgenol Radium Ther Nucl Med; 1971 Jul 27; 112(3):532-6. PubMed ID: 5570364
    [No Abstract] [Full Text] [Related]

  • 99. Brachydactyly in an Indian family.
    Mohan J.
    J Med Genet; 1969 Sep 27; 6(3):349-51. PubMed ID: 5345109
    [No Abstract] [Full Text] [Related]

  • 100. Brachydactyly with extrahepatic biliary atresia, patent ductus arteriosus and seizures--a new syndrome?
    Roper EC, Hobson EE, Sprigg A, Dobbie A, Parker MJ.
    Clin Dysmorphol; 2005 Jul 27; 14(3):117-121. PubMed ID: 15930899
    [Abstract] [Full Text] [Related]

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