These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

255 related articles for article (PubMed ID: 30204977)

  • 1. 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
    [No Abstract]   [Full Text] [Related]  

  • 2. Incidental finding of paternal UPD15 in a child with a deletion of 11q21-q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features.
    Tucker T; Steinraths M; Oh T; Nelson TN; Van Allen MI; Brown L; Schlade-Bartusiak K
    Clin Dysmorphol; 2016 Apr; 25(2):77-81. PubMed ID: 26636500
    [No Abstract]   [Full Text] [Related]  

  • 3. Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review.
    Sun S; Zhan F; Jiang J; Zhang X; Yan L; Cai W; Liu H; Cao D
    BMC Med Genomics; 2019 Dec; 12(1):197. PubMed ID: 31864361
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
    Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
    Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fetal trisomy 8 mosaicism associated with truncus arteriosus Type I.
    Sherer DM; Dalloul M; Pinard V; Sheu J; Abulafia O
    Ultrasound Obstet Gynecol; 2017 Oct; 50(4):541-542. PubMed ID: 28093816
    [No Abstract]   [Full Text] [Related]  

  • 6. Constitutional Trisomy 8 Mosaicism with Persistent Macrocytosis.
    Altıner Ş; Kutlay NY; İlhan O
    Cytogenet Genome Res; 2016; 150(1):35-39. PubMed ID: 27838684
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.
    Font-Montgomery E; Stone KM; Weaver DD; Vance GH; Das S; Thurston VC
    Birth Defects Res A Clin Mol Teratol; 2005 Aug; 73(8):577-82. PubMed ID: 16007591
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Twenty-five additional cases of trisomy 9 mosaic: Birth information, medical conditions, and developmental status.
    Bruns DA; Campbell E
    Am J Med Genet A; 2015 May; 167A(5):997-1007. PubMed ID: 25755087
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21.
    Li J; Xie M; Wang F; Ma J; Li J; Chen C; Li Z; Wang J; Zhang Y; Li Y
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1279. PubMed ID: 32463164
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial trisomy 1(q42-->qter): a new case with a mild phenotype.
    Concolino D; Cinti R; Ferraro L; Moricca MT; Strisciuglio P
    J Med Genet; 1998 Jan; 35(1):75-7. PubMed ID: 9475102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [No Abstract]   [Full Text] [Related]  

  • 12. Mosaic trisomy 8 syndrome with a novel finding of ectopic kidney.
    Aykut A; Cogulu O; Ozkinay F
    Genet Couns; 2012; 23(1):77-80. PubMed ID: 22611646
    [No Abstract]   [Full Text] [Related]  

  • 13. 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; 81(3):265-71. PubMed ID: 21204802
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Maternal uniparental disomy chromosome 14: case report and literature review.
    Falk MJ; Curtis CA; Bass NE; Zinn AB; Schwartz S
    Pediatr Neurol; 2005 Feb; 32(2):116-20. PubMed ID: 15664772
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A finding in genetic polymorphism analysis study: A case of non-mosaic 47, XXX without manifestations.
    Yang X; Ye Z; Zhang X; Wang H; Liu C
    Leg Med (Tokyo); 2017 Jul; 27():38-42. PubMed ID: 28697408
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Maternal uniparental isodisomy 11q13qter in a dysmorphic and mentally retarded female with partial trisomy mosaicism 11q13qter.
    Kotzot D; Röthlisberger B; Riegel M; Schinzel A
    J Med Genet; 2001 Dec; 38(12):876-81. PubMed ID: 11768394
    [No Abstract]   [Full Text] [Related]  

  • 17. Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X.
    Yao H; Zhang L; Zhang H; Jiang F; Hu H; Chen F; Jiang H; Mu F; Zhao L; Liang Z; Wang W
    Prenat Diagn; 2012 Nov; 32(11):1114-6. PubMed ID: 22903289
    [No Abstract]   [Full Text] [Related]  

  • 18. Rare case of XX/XY mosaicism and trisomy 13 in early prenatal diagnosis.
    Sifakis S; Anagnostopoulou K; Plastira K; Vrachnis N; Konstantinidou A; Sklavounou E
    Birth Defects Res A Clin Mol Teratol; 2012 Apr; 94(4):245-8. PubMed ID: 22282126
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Child language development delay in craniofacial dysplasia].
    Schwemmle C; Lüerssen K; Tolloczko R; Ptok M
    HNO; 2004 Feb; 52(2):150-2. PubMed ID: 14968319
    [No Abstract]   [Full Text] [Related]  

  • 20. 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
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 13.