110 related articles for article (PubMed ID: 9827922)
1. Cryptic deletions and inversions of chromosome 21 in a phenotypically normal infant with transient abnormal myelopoiesis: a molecular cytogenetic study.
Kempski HM; Craze JL; Chessells JM; Reeves BR
Br J Haematol; 1998 Nov; 103(2):473-9. PubMed ID: 9827922
[TBL] [Abstract][Full Text] [Related]
2. Myelodysplastic syndrome after regression of transient abnormal myelopoiesis in a Down syndrome infant: different clonal origin?
Kounami S; Aoyagi N; Tsuno H; Suzuki H; Kobayashi M; Koike M
Cancer Genet Cytogenet; 1998 Jul; 104(2):115-8. PubMed ID: 9666804
[TBL] [Abstract][Full Text] [Related]
3. Additional chromosome abnormalities in transient abnormal myelopoiesis in Down's syndrome patients.
Kounami S; Aoyagi N; Tsuno H; Suzuki H; Kitano N; Koike M
Acta Haematol; 1997; 98(2):109-12. PubMed ID: 9286308
[TBL] [Abstract][Full Text] [Related]
4. Trisomy 21 associated transient neonatal myeloproliferation in the absence of Down's syndrome.
Richards M; Welch J; Watmore A; Readett D; Vora AJ
Arch Dis Child Fetal Neonatal Ed; 1998 Nov; 79(3):F215-7. PubMed ID: 10194996
[TBL] [Abstract][Full Text] [Related]
5. Hypoechoic hepatomegaly associated with transient abnormal myelopoiesis provides clues to trisomy 21 in the third-trimester fetus.
Hamada H; Yamada N; Watanabe H; Okuno S; Fujiki Y; Kubo T
Ultrasound Obstet Gynecol; 2001 May; 17(5):442-4. PubMed ID: 11380972
[TBL] [Abstract][Full Text] [Related]
6. Lineage-specific trisomy 21 in a neonate with resolving transient myeloproliferative syndrome.
Slayton WB; Spangrude GJ; Chen Z; Greene WF; Virshup D
J Pediatr Hematol Oncol; 2002; 24(3):224-6. PubMed ID: 11990311
[TBL] [Abstract][Full Text] [Related]
7. Transient myeloproliferative disorder in chromosomally normal newborn infant.
Kalousek DK; Chan KW
Med Pediatr Oncol; 1987; 15(1):38-41. PubMed ID: 2951583
[TBL] [Abstract][Full Text] [Related]
8. A brief review of cryptic duplications of 21q as an emerging cause of Down syndrome: practical considerations for accurate detection.
Garcia-Heras J; Rao PN
Clin Genet; 1999 Mar; 55(3):207-11. PubMed ID: 10334476
[TBL] [Abstract][Full Text] [Related]
9. Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21.
Yuzawa K; Terui K; Toki T; Kanezaki R; Kobayashi A; Sato T; Kamio T; Kudo K; Sasaki S; Endo M; Ozono S; Nomura K; Ito E
Pediatr Blood Cancer; 2020 Apr; 67(4):e28188. PubMed ID: 32020774
[TBL] [Abstract][Full Text] [Related]
10. Inv21p12q22del21q22 and intellectual disability.
Oliveira R; Dória S; Madureira C; Lima V; Almeida C; Pinho MJ; Ramalho C; Matoso E; Barros A; Carreira IM; Moura CP
Gene; 2013 Mar; 517(1):120-4. PubMed ID: 23266646
[TBL] [Abstract][Full Text] [Related]
11. Trisomy 21 in transient myeloproliferative disorder.
Faed MJ; Robertson J; Todd AS; Sivakumaran M; Tarnow-Mordi WO
Cancer Genet Cytogenet; 1990 Sep; 48(2):259-64. PubMed ID: 2144465
[TBL] [Abstract][Full Text] [Related]
12. [Non-radioactive in situ hybridization of alpha-satellite sequences in cytogenetic diagnosis].
Perfumo C; Arslanian A; Zara F; Piombo G; Pierluigi M
Pathologica; 1992; 84(1091):363-9. PubMed ID: 1465321
[TBL] [Abstract][Full Text] [Related]
13. Transient abnormal myelopoiesis in a cytogenetically normal neonate.
Yanase K; Kato K; Katayama N; Mouri Y; Kobayashi C; Shiono J; Abe M; Yoshimi A; Koike K; Arai J; Tsuchida M
Int J Hematol; 2010 Oct; 92(3):527-30. PubMed ID: 20859711
[TBL] [Abstract][Full Text] [Related]
14. Transient abnormal myelopoiesis in a phenotypically normal newborn with polyclonal trisomy 21.
Corazza F; Astolfi A; Libri V; Franzoni M; Serravalle S; Alessandroni R; Melchionda F; Pession A
Int J Hematol; 2014 Jun; 99(6):794-7. PubMed ID: 24771229
[TBL] [Abstract][Full Text] [Related]
15. Characterization of the blast cell population in two neonates with Down's syndrome and transient myeloproliferative disorder.
Coulombel L; Derycke M; Villeval JL; Leonard C; Breton-Gorius J; Vial M; Bourgeois P; Tchernia G
Br J Haematol; 1987 May; 66(1):69-76. PubMed ID: 2954579
[TBL] [Abstract][Full Text] [Related]
16. Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization.
Tardy EP; Tóth A; Kosztolányi G
Prenat Diagn; 1997 Sep; 17(9):871-3. PubMed ID: 9316133
[TBL] [Abstract][Full Text] [Related]
17. Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome.
Abe K; Kajii T; Niikawa N
Hum Genet; 1989 Jul; 82(4):313-6. PubMed ID: 2525515
[TBL] [Abstract][Full Text] [Related]
18. Cytogenetic remission induced by interferon-alpha in a myeloproliferative disorder with trisomy 8.
Petrini M; Simi P; Saglio G
Br J Haematol; 1996 Mar; 92(4):941-3. PubMed ID: 8616089
[TBL] [Abstract][Full Text] [Related]
19. Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2.
Niikawa N; Deng HX; Abe K; Harada N; Okada T; Tsuchiya H; Akaboshi I; Matsuda I; Fukushima Y; Kaneko Y
Hum Genet; 1991 Sep; 87(5):561-6. PubMed ID: 1680787
[TBL] [Abstract][Full Text] [Related]
20. [Transient myeloproliferative disorder (TMD) with transiently increased tetrasomy-21 cells in a phenotypically normal newborn].
Takeda T; Murano K; Chihara H; Taki M; Watanabe A; Yamada K; Sugita K; Nakazawa S
Rinsho Ketsueki; 1989 Jul; 30(7):1010-5. PubMed ID: 2810785
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
