Genotype-phenotype analysis of 4q deletion syndrome: Proposal of a critical region

Chromosome 4q deletion syndrome: Narrowing the cardiovascular critical region to 4q32.2-q34.3

(2012) Wenbo Xu et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Longitudinal observation of a patient with Rieger syndrome and interstitial deletion 4 (q25-q31.1)

(2010) Lilia Moreira et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy

(2010) Mohammed Al-Owain et al.   Clinical & Developmental Immunology

Identification and molecular characterization of two novel chromosomal deletions associated with autism

(2010) W-H Chien et al.   CLINICAL GENETICS

Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech

(2010) C. Bonnet et al.   JOURNAL OF MEDICAL GENETICS

A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

(2010) R. J. L. F. Lemmers et al.   SCIENCE

Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: Study of two cases and review of the literature

(2009) Michael R. Rossi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24

(2009) Yvonne Hilhorst-Hofstee et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

DNA binding-dependent and -independent functions of the Hand2 transcription factor during mouse embryogenesis

(2009) N. Liu et al.   DEVELOPMENT

Evidence for association with hepatocellular carcinoma at the PAPSS1 locus on chromosome 4q25 in a family-based study

(2009) Wei-Liang Shih et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range

(2009) Bo Gao et al.   NATURE

Macrophages regulate salt-dependent volume and blood pressure by a vascular endothelial growth factor-C–dependent buffering mechanism

(2009) Agnes Machnik et al.   NATURE MEDICINE

Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report

(2009) Ryan N Traylor et al.   Molecular Cytogenetics

Investigation of 4q-deletion in two unrelated patients using array CGH

(2008) S.S. Kaalund et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Polycystic Kidney Disease

(2008) Peter C. Harris et al.   Annual Review of Medicine

TMC1 but Not TMC2 Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families

(2008) Abdelaziz Tlili et al.   AUDIOLOGY AND NEURO-OTOLOGY

Structural Basis for Cargo Regulation of COPII Coat Assembly

(2008) Scott M. Stagg et al.   CELL

Cardiac Neural Crest Expression of Hand2 Regulates Outflow and Second Heart Field Development

(2008) Yuka Morikawa et al.   CIRCULATION RESEARCH

Expression and function of BMP3 during chick limb development

(2008) Laura W. Gamer et al.   DEVELOPMENTAL DYNAMICS

Signal Transduction Pathway through Activin Receptors as a Therapeutic Target of Musculoskeletal Diseases and Cancer

(2008) Kunihiro TSUCHIDA et al.   ENDOCRINE JOURNAL

Neurogenin 2 controls cortical neuron migration through regulation of Rnd2

(2008) Julian Ik-Tsen Heng et al.   NATURE

TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction

(2008) A Kemal Topaloglu et al.   NATURE GENETICS

Distal del(4) (q33) syndrome: Detailed clinical presentation and molecular description with array-CGH

(2007) Sofia Kitsiou-Tzeli et al.   European Journal of Medical Genetics

Bone sialoprotein and its transcriptional regulatory mechanism

(2007) Y. Ogata   JOURNAL OF PERIODONTAL RESEARCH