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Journal Abstract Search

200 related items for PubMed ID: 10412817

  • 1. Mosaic tetrasomy 9p in a girl with multiple congenital anomalies: cytogenetic and molecular-cytogenetic studies.
    Stumm M, Tönnies H, Mandon U, Götze A, Krebs P, Wieacker PF.
    Eur J Pediatr; 1999 Jul; 158(7):571-5. PubMed ID: 10412817
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  • 2. Moving towards a syndrome: a review of 20 cases and a new case of non-mosaic tetrasomy 9p with long-term survival.
    Tonk VS.
    Clin Genet; 1997 Jul; 52(1):23-9. PubMed ID: 9272709
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  • 7. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J, Kimijima Y, Yamada S, Amagasa T, Saito-Ohara F.
    J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
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  • 9. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
    Chen CP, Lin SP, Lin YH, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
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  • 11. [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].
    Bocian E, Nowakowska B, Obersztyn E, Borg K, Chudoba I, Kostyk E, Kruczek A, Pietrzyk J, Mazurczak T.
    Med Wieku Rozwoj; 2006 Dec; 10(1 Pt 2):211-25. PubMed ID: 17028390
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  • 12. Mosaic 5p tetrasomy.
    Stanley WS, Powell CM, Devine GC, Ellingham T, Samango-Sprouse CA, Vaught DR, Murphy BA, Rosenbaum KN.
    Am J Med Genet; 1993 Mar 15; 45(6):774-6. PubMed ID: 8456861
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  • 16. Partial trisomy 15q: report of a patient and literature review.
    Chandler K, Schrander-Stumpel CT, Engelen J, Theunissen P, Fryns JP.
    Genet Couns; 1997 Mar 15; 8(2):91-7. PubMed ID: 9219006
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  • 17. Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.
    Horn D, Majewski F, Hildebrandt B, Körner H.
    J Med Genet; 1995 Jan 15; 32(1):68-71. PubMed ID: 7897632
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  • 18. Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.
    Ko JM, Kim JB, Pai KS, Yun JN, Park SJ.
    J Korean Med Sci; 2010 Dec 15; 25(12):1798-801. PubMed ID: 21165297
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  • 20. [Cytogenetic-molecular analysis of balanced chromosomal rearrangements in nine patients with intellectual disability, dysmorphic features and congenital abnormalities].
    Borg K, Bocian E, Stankiewicz P, Obersztyn E, Kruczek A, Nowakowska B, Ilnicka A, Mazurczak T.
    Med Wieku Rozwoj; 2006 Dec 15; 10(1 Pt 2):227-46. PubMed ID: 17028391
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