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Journal Abstract Search

158 related items for PubMed ID: 2407847

  • 21. Lethal evolution of a newborn with consistent features of hydrolethalus syndrome--Romanian patient.
    Belengeanu V, Viskari H, Tallila J, Lahtela J, Farcas S, Andreescu N, Stoian M, Bohiltea CL, Fryns JP.
    Genet Couns; 2011; 22(3):293-304. PubMed ID: 22029171
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  • 22. Phenotypic variability in Patau syndrome.
    Caba L, Rusu C, Butnariu L, Panzaru M, Braha E, Volosciuc M, Popescu R, Gramescu M, Bujoran C, Martiniuc V, Covic M, Gorduza EV.
    Rev Med Chir Soc Med Nat Iasi; 2013; 117(2):321-7. PubMed ID: 24340511
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  • 23. Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria.
    Sergi C, Gekas J, Kamnasaran D.
    Fetal Pediatr Pathol; 2012 Oct; 31(5):315-8. PubMed ID: 22432933
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  • 24. Prenatal detection of hydrolethalus syndrome.
    Hartikainen-Sorri AL, Kirkinen P, Herva R.
    Prenat Diagn; 1983 Jul; 3(3):219-24. PubMed ID: 6353401
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  • 25. Prenatal ultrasound findings in hydrolethalus: continuing difficulties in diagnosis.
    Norgard M, Yankowitz J, Rhead W, Kanis AB, Hall BD.
    Prenat Diagn; 1996 Feb; 16(2):173-9. PubMed ID: 8650130
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  • 26. Neu-Laxova syndrome: report of a case from Turkey.
    Kuseyri F, Bilge I, Bilgiç L, Apak MY.
    Clin Genet; 1993 May; 43(5):267-9. PubMed ID: 8375108
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  • 31. Overlap between Majewski and hydrolethalus syndromes: a report of two cases.
    Sharma AK, Phadke S, Chandra K, Upreti M, Khan EM, Naveed M, Agarwal SS.
    Am J Med Genet; 1992 Aug 01; 43(6):949-53. PubMed ID: 1415345
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  • 32. Pseudo-trisomy 13 in a fetus: further support for autosomal recessive inheritance.
    Utine GE, Alanay Y, Aktaş D, Talim B, Kale G, Tunçbilek E.
    Turk J Pediatr; 2008 Aug 01; 50(3):287-90. PubMed ID: 18773678
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  • 34. [7-week-old infant with a hydrolethalus syndrome: case report, differential diagnosis and literature review].
    Haverkamp F, Zerres K, Fahnenstich H, Köhler W, Kowalewski S.
    Klin Padiatr; 1990 Aug 01; 202(6):387-90. PubMed ID: 2266703
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  • 36. Megalencephaly and polymicrogyria with polydactyly syndrome.
    Tohyama J, Akasaka N, Saito N, Yoshimura J, Nishiyama K, Kato M.
    Pediatr Neurol; 2007 Aug 01; 37(2):148-51. PubMed ID: 17675034
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  • 37. Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome).
    Verloes A, Gillerot Y, Walczak E, Van Maldergem L, Koulischer L.
    Am J Med Genet; 1992 Jan 15; 42(2):180-3. PubMed ID: 1733166
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  • 38. Case report: two patients with oculocerebrocutaneous syndrome and terminal digital amputations.
    Asher NG, Olney AH, Schaefer GB.
    Semin Pediatr Neurol; 2008 Dec 15; 15(4):221-3. PubMed ID: 19073332
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  • 39. Pathologic features in two siblings with the Pena-Shokeir I syndrome.
    Bisceglia M, Zelante L, Bosman C, Cera R, Dallapiccola B.
    Eur J Pediatr; 1987 May 15; 146(3):283-7. PubMed ID: 3595647
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