SCOPUS 정보 검색 플랫폼

Volumn 104, Issue 4, 2001, Pages 307-311

FISH analysis for apparently simple terminal deletions of the X chromosome: Identification of hidden structural abnormalities

(8) Ogata, Tsutomu a Matsuo, Nobutake b Fukushima, Yoshimitsu c Saito, Masakazu d Nose, Osamu e Miharu, Norio f Uehara, Shigeki g Ishizuka, Bunpei h

a KEIO UNIVERSITY (Japan)

b TOKYO ELECTRIC POWER COMPANY (Japan)

c SHINSHU UNIVERSITY SCHOOL OF MEDICINE (Japan)

d Mitsubishi Kagaku Bio Clinical Laboratories Inc (Japan)

e Nose Clinic (Japan)

f HIROSHIMA UNIV SCHOOL OF MEDICINE (Japan)

g TOHOKU UNIVERSITY SCHOOL OF MEDICINE (Japan)

h ST MARIANNA UNIVERSITY SCHOOL OF MEDICINE (Japan)

Author keywords

Clinical application; FISH; Structural analysis; X chromosome

Indexed keywords

ADULT; ARTICLE; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION X; CHROMOSOME DUPLICATION; CHROMOSOME PAINTING; CHROMOSOME REARRANGEMENT; CHROMOSOME STRUCTURE; CHROMOSOME XP; CHROMOSOME XQ; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENOTYPE; HUMAN; INTERSTITIAL CHROMOSOME DELETION; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; TELOMERE;

ADULT; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DELETION; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; X CHROMOSOME;

EID: 0035893010 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10071 Document Type: Article

Times cited : (19)

References (13)

1
- 0034612238
- Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: The Lyon repeat hypothesis
- (2000) Proc Natl Acad Sci USA , vol.97 , pp. 6634-6639
- Bailey, J.A.¹ Carrel, L.² Chakravarti, A.³ Eichler, E.E.⁴

2
- 0003671748
- New York: Wiley-Liss
- (1997) Chromosomal variation in man: a catalog of chromosomal variants and anomalies, 8th ed.
- Borgaonkar, D.B.¹

3
- 0020059758
- Clinical and cytogenetic aspects of X-chromosome deletions
- (1982) Clin Genet , vol.21 , pp. 36-52
- Goldman, B.¹ Polani, P.E.² Daker, M.G.³ Angell, R.R.⁴

4
- 0026906868
- Kallmann syndrome due to a translocation resulting in an X/Y fusion gene
- (1992) Nat Genet , vol.1 , pp. 337-340
- Guioli, S.¹ Incerti, B.² Zanaria, E.³ Bardoni, B.⁴ Franco, B.⁵ Taylor, K.⁶ Ballabio, A.⁷ Camerino, G.⁸

5
- 0029671116
- An analysis of Xq deletions
- (1996) Hum Genet , vol.97 , pp. 375-381
- Maraschio, P.¹ Tupler, R.² Barbierato, L.³ Dainotti, E.⁴ Larizza, D.⁵ Bernardi, F.⁶ Hoeller, H.⁷ Garau, A.⁸ Tiepolo, L.⁹

6
- 0032769462
- Random X-inactivation in a girl with duplication Xp11.21-p21.3: Report of a patient and review of the literature
- (1999) Am J Med Genet , vol.86 , pp. 44-50
- Matsuo, M.¹ Muroya, K.² Kosaki, K.³ Ishii, T.⁴ Fukushima, Y.⁵ Anzo, M.⁶ Ogata, T.⁷

7
- 16044371402
- A complete set of human telomeric probes and their clinical application
- (1996) Nat Genet , vol.14 , pp. 86-89
- Ning, Y.¹ Roschke, A.² Smith, A.C.M.³ Macha, M.⁴ Precht, K.⁵ Riethman, H.⁶ Ledbetter, D.H.⁷ Flint, J.⁸ Horsley, S.⁹ Regan, R.¹⁰ Kearney, L.¹¹ Knight, S.¹² Kvaloy, K.¹³ Brown, W.R.A.¹⁴

8
- 0034456564
- Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature
- (2000) J Clin Endocrinol Metab , vol.85 , pp. 2927-2930
- Ogata, T.¹ Kosho, T.² Wakui, K.³ Fukushima, Y.⁴ Yoshimoto, M.⁵ Miharu, N.⁶

9
- 0030940217
- Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
- (1997) Nat Genet , vol.16 , pp. 54-63
- Rao, E.¹ Weiss, B.² Fukami, M.³ Rump, A.⁴ Niesler, B.⁵ Mertz, A.⁶ Muroya, K.⁷ Binder, G.⁸ Kirsch, S.⁹ Winkelmann, M.¹⁰ Nordsiek, G.¹¹ Heinrich, U.¹² Breuning, M.H.¹³ Ranke, M.B.¹⁴ Rosenthal, A.¹⁵ Ogata, T.¹⁶ Rappold, G.¹⁷

10
- 0023646823
- A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination
- (1987) Cell , vol.51 , pp. 417-425
- Rouyer, F.¹ Simmler, M.C.² Page, D.C.³ Weissenbach, J.⁴

11
- 0030828763
- Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females
- (1997) Hum Mol Genet , vol.6 , pp. 1985-1989
- Schiebel, K.¹ Winkelmann, M.² Mertz, A.³ Xu, X.⁴ Page, D.C.⁵ Weil, D.⁶ Petit, C.⁷ Rappold, G.A.⁸

12
- 0003145436
- Longitudinal standards for height and height velocity for Japanese children from birth to maturity
- (1992) Clin Pediatr Endocrinol , vol.1 , pp. 5-14
- Suwa, S.¹ Tachibana, K.² Maesaka, H.³ Tanaka, T.⁴ Yokoya, S.⁵

13
- 0029656085
- Molecular definition of breakpoints associated with human Xq isochromosomes: Implications for mechanisms of formation
- (1996) Am J Hum Genet , vol.58 , pp. 154-160
- Wolff, D.J.¹ Miller, A.P.² Van Dyke, D.L.³ Schwartz, S.⁴ Willard, H.F.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.