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。Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary Teeth
Pekka Nieminen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
CEP152 is a genome maintenance protein disrupted in Seckel syndrome
Ersan Kalay et al.
NATURE GENETICS (2011)
Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy
Konstantinos Nikopoulos et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia
Sascha Vermeer et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Exome sequencing identifies the cause of a mendelian disorder
Sarah B. Ng et al.
NATURE GENETICS (2010)
ALX4 dysfunction disrupts craniofacial and epidermal development
Hulya Kayserili et al.
HUMAN MOLECULAR GENETICS (2009)
Skewed X inactivation in an X linked nystagmus family resulted from a novel, p.R229G, missense mutation in the FRMD7 gene
Y. Kaplan et al.
BRITISH JOURNAL OF OPHTHALMOLOGY (2008)
Interleukin-11 receptor signaling is required for normal bone remodeling
NA Sims et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2005)
The zebrafish (Danio rerio): a model system for cranial suture Patterning
N Quarto et al.
CELLS TISSUES ORGANS (2005)
Interleukin-6 and interleukin-11 support human osteoclast formation by a RANKL-independent mechanism
O Kudo et al.
BONE (2003)
Malformations of the craniofacial region: Evolutionary, embryonic, genetic, and clinical perspectives
MM Cohen
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Sensitive nonradioactive detection of mRNA in tissue sections: Novel application of the whole-mount in situ hybridization protocol
AFM Moorman et al.
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY (2001)
分享论文
