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Journal Abstract Search

115 related items for PubMed ID: 22611646

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  • 2. Ring chromosome 8 with mosaic trisomy 8 syndrome in an infant.
    Imataka G, Ishii J, Tsukada K, Suzumura H, Arisaka O.
    Genet Couns; 2013; 24(4):441-4. PubMed ID: 24551990
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  • 3. DOUBLE TRISOMY MOSAICISM 48,XXX,+8/46,XX IN A FEMALE: THE FIRST REPORTED CASE.
    Attig A, Ben Jemaa L, Kraoua L, Jilani H, Maazoul F, Mrad R.
    Genet Couns; 2016; 27(3):441-446. PubMed ID: 30204977
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  • 7. Bilateral severe microphthalmia in a neonate with trisomy 8 mosaicism: A new finding.
    Sanderson B, Leach C, Zein M, Islam O, MacLean G, Strube YNJ, Guerin A.
    Am J Med Genet A; 2021 Feb; 185(2):534-538. PubMed ID: 33179440
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  • 9. Transfusion medicine illustrated: Mosaic Trisomy 9 in an infant with mixed-field ABO blood grouping.
    Lockhart EL, Combs MR, Buck A, Horn S, Deak K.
    Transfusion; 2013 Sep; 53(9):1884. PubMed ID: 24015938
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  • 10. Constitutional Trisomy 8 Mosaicism with Persistent Macrocytosis.
    Altıner Ş, Kutlay NY, İlhan O.
    Cytogenet Genome Res; 2016 Sep; 150(1):35-39. PubMed ID: 27838684
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  • 11. A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical description of Warkany-Down syndrome and mechanism of origin.
    McGregor-Schuerman M, Lo Fo Sang A, Bihari S, Ramdajal N, Suijkerbuijk RF, van Ravenswaaij-Arts CM.
    Eur J Med Genet; 2020 Jun; 63(6):103922. PubMed ID: 32240827
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  • 14. Patterned hypopigmentation associated with prenatally diagnosed trisomy 7 mosaicism: long-term follow-up.
    Di Lernia V.
    J Dtsch Dermatol Ges; 2015 Sep; 13(9):914-6. PubMed ID: 26283298
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  • 15. Disappearance of the trisomy 15 cell line at long-term follow-up in mosaic trisomy 15 at amniocentesis.
    Chen CP.
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):373. PubMed ID: 33678347
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  • 17. Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetus.
    Schlegel M, Baumer A, Riegel M, Wiedemann U, Schinzel A.
    Prenat Diagn; 2002 May; 22(5):418-21. PubMed ID: 12001199
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  • 18. Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome.
    Flori E, Girodon E, Samama B, Becmeur F, Viville B, Girard-Lemaire F, Doray B, Schluth C, Marcellin L, Boehm N, Goossens M, Pingault V.
    Eur J Hum Genet; 2005 Sep; 13(9):1013-8. PubMed ID: 15915162
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  • 19. Pigmentary mosaicism with trisomy 7.
    Park MY, Jin H, You HS, Shim WH, Kim GW, Kim HS, Kim BS, Kim MB, Ko HC.
    J Dermatol; 2018 Feb; 45(2):e47-e48. PubMed ID: 29047159
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  • 20. An infant with trisomy 15 mosaicism.
    Isikay S, Carman KB.
    Clin Dysmorphol; 2013 Oct; 22(4):172-174. PubMed ID: 24326963
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