Two sisters with Rett syndrome and different deletions in the MECP2 gene

被引：0

作者：

Lazarou, Lazarus ^{[1
]}

Mckee, S. A. ^{[2
]}

Rosser, L. ^{[1
]}

Cooper, D. ^{[3
]}

Hughes, J. ^{[4
]}

Butler, R. ^{[1
]}

机构：

[1] Univ Wales Hosp, Inst Med Genet, Cardiff, Wales

[2] Belfast City Hosp, No Ireland Reg Genet Ctr, Belfast BT9 7AD, Antrim, North Ireland

[3] Cardiff Univ, Inst Med Genet, Cardiff, Wales

[4] Daisy Hill Hosp, Dept Paediat, Newry, North Ireland

来源：

JOURNAL OF MEDICAL GENETICS | 2007年 / 44卷

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：S99 / S99

页数：1

共 50 条

[1] Rett syndrome and the MECP2 gene
Webb, T
Latif, F
JOURNAL OF MEDICAL GENETICS, 2001, 38 (04) : 217 - 223
[2] Large deletions of the MECP2 gene in Chinese patients with classical Rett syndrome
Pan, H.
Li, M-R
Nelson, P.
Bao, X-H
Wu, X-R
Yu, S.
CLINICAL GENETICS, 2006, 70 (05) : 418 - 419
[3] Mutations of the MECP2 gene in Rett syndrome
Hampson, K
Latif, F
Woods, CG
Webb, T
JOURNAL OF MEDICAL GENETICS, 2000, 37 : S73 - S73
[4] Characterization of large deletions of the MECP2 gene in Rett syndrome patients by gene dosage analysis
Vidal, Silvia
Pascual-Alonso, Ainhoa
Rabaza-Gairi, Marc
Gerotina, Edgar
Brandi, Nuria
Pacheco, Paola
Xiol, Clara
Pineda, Merce
Armstrong, Judith
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (08):
[5] Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome
Laccone, F
Jünemann, I
Whatley, S
Morgan, R
Butler, R
Huppke, P
Ravine, D
HUMAN MUTATION, 2004, 23 (03) : 234 - 244
[6] Two novel mutations in the MECP2 gene in patients with Rett syndrome
Alashti, Shayan Khalili
Fallahi, Jafar
Mohammadi, Sanaz
Dehghanian, Fatemeh
Farbood, Zahra
Masoudi, Marjan
Poorang, Shiva
Jokar, Arezoo
Fardaei, Majid
GENE, 2020, 732
[7] Rett Syndrome and MeCP2
Liyanage, Vichithra R. B.
Rastegar, Mojgan
NEUROMOLECULAR MEDICINE, 2014, 16 (02) : 231 - 264
[8] Rett Syndrome and MeCP2
Vichithra R. B. Liyanage
Mojgan Rastegar
NeuroMolecular Medicine, 2014, 16 : 231 - 264
[9] MECP2 deletions and genotype-phenotype correlation in Rett syndrome
Scala, Elisa
Longo, Ilaria
Ottimo, Federica
Speciale, Caterina
Sampieri, Katia
Katzaki, Eleni
Artuso, Rosangela
Mencarelli, Maria Antonietta
D'Ambrogio, Tatiana
Vonella, Giuseppina
Zappella, Michele
Hayek, Giuseppe
Battaglia, Agatino
Mari, Francesca
Renieri, Alessandra
Ariani, Francesca
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2007, 143A (23) : 2775 - 2784
[10] Novel double deletions in the MECP2 gene in Tunisian Rett patient
Fendri-Kriaa, Nourhene
Rouissi, Aida
Ghorbel, Rania
Mkaouar-Rebai, Emna
Belguith, Neila
Gouider-Khouja, Naziha
Fakhfakh, Faiza
GENE, 2012, 502 (02) : 163 - 167

← 1 2 3 4 5 →