SCOPUS 정보 검색 플랫폼

Prenatal Diagnosis

Volumn 21, Issue 2, 2001, Pages 96-98

Acrocentric chromosome polymorphisms: Beware of cryptic translocations

(4) Petignat, Patrick a Vial, Yvan a Laurini, Richard a Hohlfeld, Patrick a

a LAUSANNE UNIVERSITY HOSPITAL (Switzerland)

Author keywords

Acrocentic short arm; Beckwith Wiedemann syndrome (BWS); Trisomy 11p15.5

Indexed keywords

ACROCENTRIC CHROMOSOME; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CHROMOSOME 14P; CHROMOSOME ANALYSIS; CHROMOSOME NOR; CHROMOSOME POLYMORPHISM; CHROMOSOME TRANSLOCATION 11; CLINICAL FEATURE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY;

ADULT; BECKWITH-WIEDEMANN SYNDROME; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 14; COLORING AGENTS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; NUCLEOLUS ORGANIZER REGION; POLYMORPHISM, GENETIC; PREGNANCY; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0035099924 PISSN: 01973851 EISSN: None Source Type: Journal
DOI: 10.1002/1097-0223(200102)21:2<96::AID-PD986>3.0.CO;2-O Document Type: Article

Times cited : (12)

References (10)

1
- 0032057260
- Characterization of the breakpoints in unbalanced t(5;11) (p15;p15) constitutional chromosome translocations in two patients with Beckwith-Wiedemann syndrome using fluorescence in situ hybridization
- (1998) Int J Mol Med , vol.1 , pp. 801-808
- Grundy, R.G.¹ Aledo, R.² Cowell, J.K.³

2
- 16044364516
- kip2 is mutated in Beckwith-Wiedemann syndrome
- (1996) Nat Genet , vol.14 , pp. 171-173
- Hatada, I.¹ Ohashi, H.² Fukushima, Y.³

3
- 0029762721
- A new case of Beckwith-Wiedemann syndrome with an 11p15 duplication of paternal origin
- [46,XY, -21, +der(21), t(11;21) (p15.2;q22.3) pat]
- (1996) Acta Genet Med Gemellol (Roma) , vol.45 , pp. 245-250
- Krajewska-Walasek, M.¹ Gutkowska, A.² Mospinek-Krasnopolska, M.³ Chrzanowska, K.⁴

4
- 0032475940
- Molecular genetics of Wiedemann-Beckwith syndrome
- (1998) Am J Med Genet , vol.79 , pp. 253-259
- Li, M.¹ Squire, J.A.² Weksberg, R.³

5
- 0031127744
- Intrauterine growth and ultrasound findings in fetuses with Beckwith-Wiedemann syndrome
- (1997) Obstet Gynecol , vol.89 , pp. 538-542
- Ranzini, A.C.¹ Day-Salvatore, D.² Turner, T.³ Smulian, J.C.⁴ Vintzileos, A.M.⁵

6
- 0030929370
- The Beckwith-Wiedemann syndrome phenotype and the risk of cancer
- (1997) Med Pediatr Oncol , vol.28 , pp. 411-415
- Schneid, H.¹ Vazquez, M.P.² Vacher, C.³ Gourmelon, M.⁴ Cabrol, S.⁵ Le Bouc, Y.⁶

7
- 0030823992
- Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome
- (1997) J Med Genet , vol.34 , pp. 819-826
- Slavotinek, A.¹ Gaunt, L.² Donnai, D.³

8
- 0030735169
- Transactivation of Igf2 in a mouse of Beckwith-Wiedemann syndrome
- (1997) Nature , vol.389 , pp. 809-815
- Sun, F.L.¹ Dean, W.L.² Kelsey, G.³ Allen, N.D.⁴ Reik, W.⁵

9
- 0031062973
- Beckwith-Wiedemann syndrome and Wilms'tumour
- (1997) Mol Hum Reprod , vol.3 , pp. 157-168
- Ward, A.¹

10
- 0027289089
- Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted
- (1993) Hum Mol Genet , vol.2 , pp. 549-556
- Weksberg, R.¹ Teshima, I.² Williams, B.R.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.