Array-comparative genomic hybridization analysis in patients with Müllerian fusion anomalies
出版年份 2018 全文链接
标题
Array-comparative genomic hybridization analysis in patients with Müllerian fusion anomalies
作者
关键词
-
出版物
CLINICAL GENETICS
Volume 93, Issue 3, Pages 640-646
出版商
Wiley
发表日期
2017-10-25
DOI
10.1111/cge.13160
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mutations inWNT9Bare associated with Mayer-Rokitansky-Küster-Hauser syndrome
- (2016) D.E.J. Waschk et al. CLINICAL GENETICS
- Variations in RBM8A and TBX6 are associated with disorders of the müllerian ducts
- (2015) Ann-Christin Tewes et al. FERTILITY AND STERILITY
- Reply to Pembrey et al: ‘ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis’
- (2014) Fabiola Ceroni et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1)
- (2013) Chih-Ping Chen et al. GENE
- TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia
- (2013) Maria Sandbacka et al. Orphanet Journal of Rare Diseases
- Frame shift mutation of LHX1 is associated with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome
- (2012) S. Ledig et al. HUMAN REPRODUCTION
- Mutations in WNT4 are not responsible for Müllerian duct abnormalities in Chinese women
- (2012) Xinyue Chang et al. REPRODUCTIVE BIOMEDICINE ONLINE
- PAX2 in 192 Chinese women with Müllerian duct abnormalities: mutation analysis
- (2012) Peng Wang et al. REPRODUCTIVE BIOMEDICINE ONLINE
- Clinical utility gene card for: Mayer–Rokitansky–Küster–Hauser syndrome
- (2011) Karine Morcel et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- High incidence of recurrent copy number variants in patients with isolated and syndromic Mullerian aplasia
- (2011) S. Nik-Zainal et al. JOURNAL OF MEDICAL GENETICS
- Derlin-2-Deficient Mice Reveal an Essential Role for Protein Dislocation in Chondrocytes
- (2011) S. K. Dougan et al. MOLECULAR AND CELLULAR BIOLOGY
- Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci
- (2011) Karine Morcel et al. Orphanet Journal of Rare Diseases
- Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome
- (2010) Susanne Ledig et al. FERTILITY AND STERILITY
- Expanding the phenotype of 22q11 deletion syndrome: the MURCS association
- (2009) Vera Uliana et al. CLINICAL DYSMORPHOLOGY
- Identification of differentially expressed genes involved in the regression and development of the chicken Mllerian duct
- (2008) Yonju Ha et al. INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY
- RSPO4 Is the Major Gene in Autosomal-Recessive Anonychia and Mutations Cluster in the Furin-Like Cysteine-Rich Domains of the Wnt Signaling Ligand R-spondin 4
- (2007) Nadina Ortiz Brüchle et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started