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Journal Abstract Search

176 related items for PubMed ID: 21975655

  • 1. Mosaic trisomy 9 presenting with congenital heart disease, facial dysmorphism and pigmentary skin lesions: intricate issues of genetic counseling.
    Patil SJ, Ponnala R, Shah S, Dalal A.
    Indian J Pediatr; 2012 Jun; 79(6):806-9. PubMed ID: 21975655
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  • 2. Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review.
    Martínez-Hernández A, Martínez-Anaya D, Durán-McKinster C, Del Castillo-Ruiz V, Navarrete-Meneses P, Córdova EJ, Villegas-Torres BE, Ruiz-Herrera A, Juárez-Velázquez R, Yokoyama-Rebollar E, Cervantes-Barragán D, Pedraza-Meléndez A, Orozco L, Pérez-Vera P, Salas-Labadía C.
    BMC Med Genomics; 2022 Oct 31; 15(1):224. PubMed ID: 36316743
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  • 4. Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome.
    Petit F, Holder-Espinasse M, Duban-Bedu B, Bouquillon S, Boute-Benejean O, Bazin A, Rouland V, Manouvrier-Hanu S, Delobel B.
    Clin Genet; 2012 Mar 31; 81(3):265-71. PubMed ID: 21204802
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  • 5. Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus.
    Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Town DD, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2021 May 31; 60(3):534-539. PubMed ID: 33966743
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  • 7. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
    Chen CP, Lin HM, Su YN, Chern SR, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2010 Sep 31; 49(3):341-50. PubMed ID: 21056321
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  • 10. Two cases of trisomy 16 mosaicism ascertained postnatally.
    Rieubland C, Francis D, Houben L, Corrie S, Bankier A, White SM.
    Am J Med Genet A; 2009 Jul 31; 149A(7):1523-8. PubMed ID: 19533780
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  • 11. Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome.
    Chen CP, Lin SY, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2020 Mar 31; 59(2):301-305. PubMed ID: 32127154
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  • 13. BACs-on-Beads™ assay for a case of trisomy 22 confined placental mosaicism.
    Zhong G, He H, Zhong Z, Chen J.
    J Obstet Gynaecol; 2021 Jul 31; 41(5):826-827. PubMed ID: 32799711
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  • 14. Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review.
    Chen CP, Huang MC, Chern SR, Wu PS, Chen SW, Chuang TY, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2019 Sep 31; 58(5):692-697. PubMed ID: 31542095
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  • 15. Do you know this syndrome? Dyspigmentation along the Blaschko lines caused by trisomy 7 mosaicism.
    Gouveia MP, Coutinho I, Teixeira V, d'Oliveira R, Venâncio M, Moreno A.
    An Bras Dermatol; 2016 Sep 31; 91(6):837-839. PubMed ID: 28099615
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  • 16. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.
    Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2013 Sep 31; 52(3):395-400. PubMed ID: 24075380
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  • 17. 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 31; 45(2):e47-e48. PubMed ID: 29047159
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  • 18. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review.
    Chen CP, Chern SR, Chen YN, Wu PS, Yang CW, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2015 Aug 31; 54(4):426-31. PubMed ID: 26384064
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  • 19. Prenatal diagnosis and genetic counseling of low-level trisomy 9 mosaicism with a favorable outcome.
    Wang C, Chen Y, Zhao J, Xia Y.
    Taiwan J Obstet Gynecol; 2020 Sep 31; 59(5):786-787. PubMed ID: 32917340
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  • 20. Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum.
    Chen CP, Hsu CY, Chern SR, Wu PS, Chen SW, Wang W.
    Taiwan J Obstet Gynecol; 2020 Jan 31; 59(1):127-129. PubMed ID: 32039780
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