270 related articles for article (PubMed ID: 11139538)
1. Pseudo dicentric chromosome (5;21): a rare example of maternal germline mosaicism.
Engel U; Bohlander SK; Bink K; Hinney B; Laccone F; Bartels I
Hum Reprod; 2001 Jan; 16(1):63-66. PubMed ID: 11139538
[TBL] [Abstract][Full Text] [Related]
2. 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
[TBL] [Abstract][Full Text] [Related]
3. Maternal uniparental disomy for chromosome 22 in a child with generalized mosaicism for trisomy 22.
de Pater JM; Schuring-Blom GH; van den Bogaard R; van der Sijs-Bos CJ; Christiaens GC; Stoutenbeek P; Leschot NJ
Prenat Diagn; 1997 Jan; 17(1):81-6. PubMed ID: 9021833
[TBL] [Abstract][Full Text] [Related]
4. Postzygotic isochromosome formation as a cause for false-negative results from chorionic villus chromosome examinations.
Riegel M; Wisser J; Baumer A; Schinzel A
Prenat Diagn; 2006 Mar; 26(3):221-5. PubMed ID: 16475225
[TBL] [Abstract][Full Text] [Related]
5. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.
Chen CP; Tsai C; Lin MH; Chern SR; Chen SW; Lai ST; Chen WL; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Oct; 56(5):691-693. PubMed ID: 29037560
[TBL] [Abstract][Full Text] [Related]
6. Discordant prenatal diagnosis of trisomy 21 due to mosaic structural rearrangements of chromosome 21.
Brisset S; Aboura A; Audibert F; Costa JM; L'Herminé AC; Gautier V; Frydman R; Tachdjian G
Prenat Diagn; 2003 Jun; 23(6):461-9. PubMed ID: 12813759
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J
Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644
[TBL] [Abstract][Full Text] [Related]
9. Characterization of a Rare Mosaicism in Autosomal Translocation of t(5;21) Using Conventional Cytogenetics and FISH Methods.
Omori Sarabi S; Karimzad Hagh J; Behrend C; Mohseni SB; Ansari Dezfouli M; Rashidi SK; Omrani MD
Iran Biomed J; 2020 Jan; 24(1):60-3. PubMed ID: 31301695
[TBL] [Abstract][Full Text] [Related]
10. Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia.
Minelli A; Morerio C; Maserati E; Olivieri C; Panarello C; Bonvini L; Leszl A; Rosanda C; Lanino E; Danesino C; Pasquali F
Leukemia; 2001 Jun; 15(6):971-5. PubMed ID: 11417485
[TBL] [Abstract][Full Text] [Related]
11. Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen.
Schuffenhauer S; Kobelt A; Daumer-Haas C; Löffler C; Müller G; Murken J; Meitinger T
Am J Med Genet; 1996 Oct; 65(1):56-9. PubMed ID: 8914742
[TBL] [Abstract][Full Text] [Related]
12. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H
Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
[TBL] [Abstract][Full Text] [Related]
13. 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; 32(1):68-71. PubMed ID: 7897632
[TBL] [Abstract][Full Text] [Related]
14. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
Chen CP; Ko TM; Chern SR; Wu PS; Chen SW; Lai ST; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):545-549. PubMed ID: 28805616
[TBL] [Abstract][Full Text] [Related]
16. Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3).
Cervera M; Sánchez S; Molina B; Alcántara MA; Del Castillo V; Carnevale A; González-del Angel A
Am J Med Genet A; 2005 Aug; 136A(4):381-5. PubMed ID: 16001443
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Two unique patients with trisomy 18 mosaicism and molecular marker studies.
Slavotinek A; Poyser L; Wallace A; Martin F; Gaunt L; Kingston H
Am J Med Genet A; 2003 Mar; 117A(3):282-8. PubMed ID: 12599194
[TBL] [Abstract][Full Text] [Related]
20. [Chorionic villus cell culture and karyotype analysis in 1 983 cases of spontaneous miscarriage].
Yuan SM; Liao C; Li DZ; Huang JZ; Hu SY; Ke M; Zhong HZ; Yi CX
Zhonghua Fu Chan Ke Za Zhi; 2017 Jul; 52(7):461-466. PubMed ID: 28797153
[No Abstract] [Full Text] [Related]
[Next] [New Search]
