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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

116 related items for PubMed ID: 10422017

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  • 4. [Proteus syndrome. A contribution to the further differential diagnosis of congenital local gigantism].
    Trappe BO, Rupprecht E, Bosselmann E, Schaeper M, Mohnike K, Gedschold J.
    Helv Paediatr Acta; 1989 Jun; 43(5-6):473-82. PubMed ID: 2745142
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  • 6. Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition.
    Martin RA, Jones MC, Jones KL.
    Am J Med Genet; 1993 Apr 15; 46(2):129-31. PubMed ID: 8387244
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  • 7. [The heart-hand syndrome. A new variant of disorders of heart conduction and syndactylia including osseous changes in hands and feet].
    Reichenbach H, Meister EM, Theile H.
    Kinderarztl Prax; 1992 Apr 15; 60(2):54-6. PubMed ID: 1318983
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  • 10. [Cryptorchidism with didymo-epididymal dissociation and Robinow's syndrome: 2 case reports].
    Fabbro MA, D'Agostino S, Costa L, Musi L, Cappellari F.
    Pediatr Med Chir; 1997 Apr 15; 19(2):121-4. PubMed ID: 9312747
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  • 12. Lobster claw hand and foot deformity in a family.
    Bhat BV, Ashok BA, Puri RK.
    Indian Pediatr; 1987 Aug 15; 24(8):675-7. PubMed ID: 3443509
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  • 13. Mirror hands and feet.
    van Steensel MA.
    J Med Genet; 1997 Aug 15; 34(8):701-2. PubMed ID: 9279770
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  • 14. [A pedigree of split hand/split foot malformation].
    Zhou FJ, Xie WM, Zhao XR, Guo ZH.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct 15; 29(5):615-6. PubMed ID: 23042405
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  • 15. A new case of Zimmermann-Laband syndrome with mild mental retardation, asymmetry of limbs, and hypertrichosis.
    de Pina Neto JM, Soares LR, Souza AH, Petean EB, Velludo MA, de Freitas AC, Ribas JP.
    Am J Med Genet; 1988 Nov 15; 31(3):691-5. PubMed ID: 3228149
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  • 16. Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal father.
    De Smet L, Devriendt K, Fryns JP.
    Genet Couns; 2001 Nov 15; 12(3):251-4. PubMed ID: 11693788
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  • 17. Trisomy 21 in a second trimester male hydropic fetus with "Noonan-syndrome-phenotype": nuchal and thoracic lymphangiomatosis, oedema of the dorsum of hands and feet, and bicuspid pulmonary valve.
    Fryns JP, Moerman P.
    Genet Couns; 1998 Nov 15; 9(1):59-60. PubMed ID: 9555591
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  • 19. Familial distal arthrogryposis type I.
    Stoll C, Alembik Y, Dott B.
    Ann Genet; 1996 Nov 15; 39(2):75-80. PubMed ID: 8766137
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