SCOPUS 정보 검색 플랫폼

Volumn 58, Issue 3, 1996, Pages 544-550

Isolation of a cosmid clone corresponding to an inv(21) breakpoint of a patient with transient abnormal myelopoiesis

(11) Ohta, Tohru a,f Nakano, Motoi a Tsujita, Takahiro a Abe, Kyohko b Osoegawa, Kazutoyo c Yamagata, Tetsushi c Yoshiura, Koh Ichiro a Jinno, Yoshihiro a Soeda, Eiichi c Nakamura, Yusuke d Niikawa, Norio a,e

a NAGASAKI UNIVERSITY (Japan)

b Kyushu Medical Science Nagasaki Laboratory (Japan)

c INST OF PHYS AND CHEMICAL RESEARCH (Japan)

d UNIVERSITY OF TOKYO (Japan)

e NAGASAKI UNIVERSITY SCHOOL OF MEDICINE (Japan)

f CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 21Q; CHROMOSOME INVERSION; COSMID; DOWN SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MAPPING; HUMAN; LEUKEMOID REACTION; MALE; MOSAICISM; MYELOPOIESIS; NEWBORN; PRIORITY JOURNAL; SEQUENCE TAGGED SITE;

ADULT; BASE SEQUENCE; CHROMOSOME WALKING; CHROMOSOMES, HUMAN, PAIR 21; CLONING, MOLECULAR; COSMIDS; DOWN SYNDROME; FEMALE; HUMANS; INFANT, NEWBORN; INVERSION, CHROMOSOME; MALE; MOLECULAR SEQUENCE DATA; MYELOPROLIFERATIVE DISORDERS; SEQUENCE TAGGED SITES;

EID: 19144363132 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (16)

References (5)

1
- 0024361278
- Disomic homozygosity in 21-trisomic cells: A mechanism responsible for transient myeloproliferative syndrome
- Abe K, Kajii T, Niikawa N (1989) Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome. Hum Genet 82:313-316
- (1989) Hum Genet , vol.82 , pp. 313-316
- Abe, K.¹ Kajii, T.² Niikawa, N.³

2
- 0027437280
- Normal phenotype with paternal uniparental isodisomy for chromosome 21
- Blouin J-L, Avramopoulos D, Pangalos C, Antonarakis SE (1993) Normal phenotype with paternal uniparental isodisomy for chromosome 21. Am J Hum Genet 53:1074-1078
- (1993) Am J Hum Genet , vol.53 , pp. 1074-1078
- Blouin, J.-L.¹ Avramopoulos, D.² Pangalos, C.³ Antonarakis, S.E.⁴

3
- 0026738541
- Continuum of overlapping clones spanning the entire human chromosome 21q
- Chumakov I, Rigault P, Guillou S, Ougen P, Billaut A, Guasconi G, Gervy P, et al (1992) Continuum of overlapping clones spanning the entire human chromosome 21q. Nature 359:380-387
- (1992) Nature , vol.359 , pp. 380-387
- Chumakov, I.¹ Rigault, P.² Guillou, S.³ Ougen, P.⁴ Billaut, A.⁵ Guasconi, G.⁶ Gervy, P.⁷

4
- 0023216251
- Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism
- Creau-Goldberg N, Gegonne A, Delabar J, Cochet C, Cabanis MO, Stehelin D, Turleau C, et al (1987) Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism. Hum Genet 76:396-398
- (1987) Hum Genet , vol.76 , pp. 396-398
- Creau-Goldberg, N.¹ Gegonne, A.² Delabar, J.³ Cochet, C.⁴ Cabanis, M.O.⁵ Stehelin, D.⁶ Turleau, C.⁷

5
- 0028145950
- Cloning and characterization of a 135- To 500-kb region of homology on the long arm of human chromosome 21
- Dutriaux A, Rossier J, Van Hul W, Nizetic D, Theophille D, Delabar JM, Van Broeckhoven C, et al (1994) Cloning and characterization of a 135- to 500-kb region of homology on the long arm of human chromosome 21. Genomics 22:472-477
- (1994) Genomics , vol.22 , pp. 472-477
- Dutriaux, A.¹ Rossier, J.² Van Hul, W.³ Nizetic, D.⁴ Theophille, D.⁵ Delabar, J.M.⁶ Van Broeckhoven, C.⁷

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.