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 *

209 related articles for article (PubMed ID: 11768394)

  • 21. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
    Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT
    Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Uniparental disomy and the phenotype of mosaic trisomy 20: a new case and review of the literature.
    Powis Z; Erickson RP
    J Appl Genet; 2009; 50(3):293-6. PubMed ID: 19638687
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Trisomy 12 mosaicism confirmed in multiple organs from a liveborn child.
    DeLozier-Blanchet CD; Roeder E; Denis-Arrue R; Blouin JL; Low J; Fisher J; Scharnhorst D; Curry CJ
    Am J Med Genet; 2000 Dec; 95(5):444-9. PubMed ID: 11146464
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism.
    Faivre L; Viot G; Prieur M; Turleau C; Gosset P; Romana S; Munnich A; Vekemans M; Cormier-Daire V
    Am J Med Genet; 2000 Apr; 91(4):273-6. PubMed ID: 10766982
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.
    Genuardi M; Tozzi C; Pomponi MG; Stagni ML; Della Monica M; Scarano G; Calvieri F; Torrisi L; Neri G
    Eur J Hum Genet; 1999; 7(4):421-6. PubMed ID: 10352932
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis.
    Velissariou V; Antoniadi T; Gyftodimou J; Bakou K; Grigoriadou M; Christopoulou S; Hatzipouliou A; Donoghue J; Karatzis P; Katsarou E; Petersen MB
    Eur J Hum Genet; 2002 Nov; 10(11):694-8. PubMed ID: 12404100
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Partial paternal uniparental disomy of chromosome 6 in an infant with neonatal diabetes, macroglossia, and craniofacial abnormalities.
    Das S; Lese CM; Song M; Jensen JL; Wells LA; Barnoski BL; Roseberry JA; Camacho JM; Ledbetter DH; Schnur RE
    Am J Hum Genet; 2000 Dec; 67(6):1586-91. PubMed ID: 11038325
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
    Schinzel A; Kotzot D; Brecevic L; Robinson WP; Dutly F; Dauwerse H; Binkert F; Baumer A; Ausserer B
    Eur J Hum Genet; 1997; 5(5):308-14. PubMed ID: 9412788
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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
    [No Abstract]   [Full Text] [Related]  

  • 33. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
    Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
    J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Trisomy 10 mosaicism and maternal uniparental disomy 10 in a liveborn infant with severe congenital malformations.
    Hahnemann JM; Nir M; Friberg M; Engel U; Bugge M
    Am J Med Genet A; 2005 Oct; 138A(2):150-4. PubMed ID: 16114048
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Supernumerary marker chromosomes (SMC) and uniparental disomy (UPD): coincidence or consequence?
    Kotzot D
    J Med Genet; 2002 Oct; 39(10):775-8. PubMed ID: 12362039
    [No Abstract]   [Full Text] [Related]  

  • 36. A rare case: mosaic trisomy 22.
    Basaran N; Berkil H; Ay N; Durak B; Ataman C; Ozdemir M; Ozon YH; Kaya I
    Ann Genet; 2001; 44(4):183-6. PubMed ID: 11755102
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mosaic maternal uniparental isodisomy for chromosome 7q21-qter.
    Reboul MP; Tandonnet O; Biteau N; Belet-de Putter C; Rebouissoux L; Moradkhani K; Vu PY; Saura R; Arveiler B; Lacombe D; Taine L; Iron A
    Clin Genet; 2006 Sep; 70(3):207-13. PubMed ID: 16922723
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
    J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A severely short-statured girl with 47,XX, + 14/46,XX,upd(14)mat, mosaicism.
    Ushijima K; Yatsuga S; Matsumoto T; Nakamura A; Fukami M; Kagami M
    J Hum Genet; 2018 Mar; 63(3):377-381. PubMed ID: 29311684
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.
    Devriendt K; Matthijs G; Claes S; Legius E; Proesmans W; Cassiman JJ; Fryns JP
    J Med Genet; 1997 Apr; 34(4):318-22. PubMed ID: 9138157
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.