Erratum to: A de novo 3p13 deletion induced by a complex chromosomal rearrangement combined with a pericentric inversion of chromosome 3, inv(3)(p13q12), and a translocation between chromosome 3 and 8, t(3;8)(q13.1;q24.2), in a child with developmental delay

被引：0

作者：

Kye Hee Cho

Sung Han Shim

MinYoung Kim

机构：

[1] CHA University,Genetics Laboratory, Fertility Center, CHA Gangnam Medical Center

[2] CHA University,Department of Rehabilitation Medicine, CHA Bundang Medical Center

来源：

Genes & Genomics | 2017年 / 39卷

关键词：

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：243 / 243

共 42 条

[21] DETAILED GENETIC AND PHYSICAL MAP OF THE 3P-CHROMOSOME REGION SURROUNDING THE FAMILIAL RENAL-CELL CARCINOMA CHROMOSOME-TRANSLOCATION, T(3,8)(P14.2,Q24.1)
LAFORGIA, S
LASOTA, J
LATIF, F
BOGHOSIANSELL, L
KASTURY, K
OHTA, M
DRUCK, T
ATCHISON, L
CANNIZZARO, LA
BARNEA, G
SCHLESSINGER, J
MODI, W
KUZMIN, I
TORY, K
ZBAR, B
CROCE, CM
LERMAN, M
HUEBNER, K
CANCER RESEARCH, 1993, 53 (13) : 3118 - 3124
[22] A small supernumerary marker chromosome resulting from a balanced maternal translocation and leading to partial trisomy of 13q12-q21.1 and 3p26.3 in a child with syndromic intellectual disability
Maazoun, Fatma
Bouhlel, Mohamed Ali
Lajmi, Yosra
Lebbar, Aziza
Ben Ayed, Ikhlas
Boujelbene, Imene
Gharbi, Nourhene
Kamoun, Hassen
Dupont, Jean-Michel
Abdelhedi, Fatma
EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 175 - 176
[23] On the prevalence of the PAX8-PPARG fusion resulting from the chromosomal translocation t(2;3)(q13;p25) in adenomas of the thyroid
Klemke, Markus
Drieschner, Norbert
Laabs, Anne
Rippe, Volkhard
Belge, Gazanfer
Bullerdiek, Joern
Sendt, Wolfgang
CANCER GENETICS, 2011, 204 (06) : 334 - 339
[24] Molecular study of a new family with hereditary renal cell carcinoma and a translocation t(3;8)(p13;q24.1)
Meléndez, B
Rodríguez-Perales, S
Martínez-Delgado, B
Otero, I
Robledo, M
Martínez-Ramirez, A
Ruiz-Llorente, S
Urioste, M
Cigudosa, JC
Benítez, J
HUMAN GENETICS, 2003, 112 (02) : 178 - 185
[25] Molecular study of a new family with hereditary renal cell carcinoma and a translocation t(3;8)(p13;q24.1)
Bárbara Meléndez
Sandra Rodríguez-Perales
Beatriz Martínez-Delgado
Ignacio Otero
Mercedes Robledo
Angel Martínez-Ramírez
Sergio Ruiz-Llorente
Miguel Urioste
Juan Cruz Cigudosa
Javier Benítez
Human Genetics, 2003, 112 : 178 - 185
[26] 2 CASES OF UNBALANCED X-A TRANSLOCATION (ONE WITH 3P-TRISOMY, ONE WITH 13Q-TRISOMY) - 46X, DEL(XQ) INV(X) (Q11Q22), T(X-3) (XPTER-]XQ11-XQ22-]XQ11-3P21-]3PTR), 46X, DIR INS(X-13)(Q25-Q12Q34)
YOSHIDA, Y
MATSUMOTO, N
FUJITA, H
TANIGAWA, Y
KIBATA, K
HAYASHI, M
JAPANESE JOURNAL OF HUMAN GENETICS, 1981, 26 (02): : 192 - 192
[27] Sperm FISH analysis of a 46,XY,t(3;6)(p24;p21.2),inv (8)(p11;2q21.2) double chromosomal rearrangement
Ferfouri, Fatma
Boitrelle, Florence
Tapia, Sylvie
Gomes, Denise Molina
Selva, Jacqueline
Vialard, Francois
REPRODUCTIVE BIOMEDICINE ONLINE, 2012, 24 (02) : 219 - 223
[28] A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9
Boyadjiev, SA
South, ST
Radford, CL
Patel, A
Zhang, G
Hur, DJ
Thomas, GH
Gearhart, JP
Stetten, G
GENOMICS, 2005, 85 (05) : 622 - 629
[29] Myeloid neoplasms associated with t(3;12)(q26.2;p13) are clinically aggressive, show myelodysplasia, and frequently harbor chromosome 7 abnormalities
Ronaghy, Arash
Hu, Shimin
Tang, Zhenya
Wang, Wei
Tang, Guilin
Loghavi, Sanam
Li, Shaoying
Thakral, Beenu
Medeiros, L. Jeffrey
Muzzafar, Tariq
MODERN PATHOLOGY, 2021, 34 (02) : 300 - 313
[30] Novel TNS3-MAP3K3 and ZFPM2-ELF5 fusion genes identified by RNA sequencing in multicystic mesothelioma with t(7;17)(p12;q23) and t(8;11)(q23;p13)
Panagopoulos, Ioannis
Gorunova, Ludmila
Davidson, Ben
Heim, Sverre
CANCER LETTERS, 2015, 357 (02) : 502 - 509

← 1 2 3 4 5 →