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。Molecular Cytogenetic and Clinical Characterization of a Patient With a 5.6-Mb Deletion in 7p15 Including HOXA Cluster
Kyung Ran Jun et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)
Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta
Pablo Lapunzina et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Proximal interstitial 1p36 deletion syndrome: The most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2)
Keiko Shimojima et al.
BRAIN & DEVELOPMENT (2009)
Natural mutations of the anti-Mullerian hormone type II receptor found in persistent Mullerian duct syndrome affect ligand binding, signal transduction and cellular transport
Corinne Belville et al.
HUMAN MOLECULAR GENETICS (2009)
A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family
Fatemeh Alasti et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
The clinical spectrum of homozygous HOXA1 mutations
Thomas M. Bosley et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5′ end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations
Ying Yue et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2007)
Breakpoints around the HOXD cluster result in various limb malformations
B Dlugaszewska et al.
JOURNAL OF MEDICAL GENETICS (2006)
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development
MA Tischfield et al.
NATURE GENETICS (2005)
Molecules mimicking Smad1 interacting with hox stimulate bone formation
ZY Liu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease
AE Shrimpton et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects
F Spitz et al.
GENOMICS (2002)
Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation
AA Thompson et al.
NATURE GENETICS (2000)
Hox C cluster genes are dispensable for overall body plan of mouse embryonic development
H Suemori et al.
DEVELOPMENTAL BIOLOGY (2000)