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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

146 related items for PubMed ID: 5031984

  • 1. Camptobrachydactyly: a new autosomal dominant trait with two probable homozygotes.
    Edwards JA, Gale RP.
    Am J Hum Genet; 1972 Jul; 24(4):464-74. PubMed ID: 5031984
    [No Abstract] [Full Text] [Related]

  • 2. Brachydactyly with absence of middle phalanges and hypoplastic nails. A new hereditary syndrome.
    Cuevas-Sosa A, García-Segur F.
    J Bone Joint Surg Br; 1971 Feb; 53(1):101-5. PubMed ID: 4325377
    [No Abstract] [Full Text] [Related]

  • 3. Six generations of a family with multiple limb deficiencies.
    Helal A, Perry T, Ogden JA, Greene TL.
    J Pediatr Orthop; 1993 Feb; 13(2):210-3. PubMed ID: 8459013
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  • 8. [A case of congenital hypodactyly of the hand and foot].
    Mamedov AG, Seidov MM.
    Ortop Travmatol Protez; 1991 Apr; (4):51-2. PubMed ID: 1754179
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  • 9. Polydactyly, conical teeth, nail dysplasia, and short limbs: a new autosomal dominant malformation syndrome.
    Curry CJ, Hall BD.
    Birth Defects Orig Artic Ser; 1979 Apr; 15(5B):253-63. PubMed ID: 526581
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  • 12. The hand-foot-uterus syndrome: a case study.
    Longmuir GA, Conley RN, Nicholson DL, Whitehead M.
    J Manipulative Physiol Ther; 1986 Sep; 9(3):213-7. PubMed ID: 3772265
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  • 13. Roentgenographic manifestations of hereditary peripheral dysostosis.
    Newcombe DS, Keats TE.
    Am J Roentgenol Radium Ther Nucl Med; 1969 May; 106(1):178-89. PubMed ID: 5769301
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  • 14. Dominant inheritance of syn-camptodactyly of the second and third toes with foot and lower limb asymmetry and scoliosis.
    Halal F.
    Am J Med Genet; 1985 Sep; 22(1):149-56. PubMed ID: 4050850
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  • 16. 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
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  • 17. Further data on acheiropody.
    Toledo SP, Saldanha PH, Borelli A, Cintra AB.
    J Genet Hum; 1972 Sep; 20(3):253-8. PubMed ID: 4659166
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  • 20. Mental retardation with absent fifth fingernail and terminal phalanx.
    Coffin GS, Siris E.
    Am J Dis Child; 1970 May; 119(5):433-9. PubMed ID: 5442442
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