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Publications by Caroline B Michielse
Refinement of the Locus for Hereditary Congenital Facial Palsy on Chromosome 3q21 in Two Unrelated Families and Screening of Positional Candidate Genes
European Journal of Human Genetics
Genetics
Insight Into the Molecular Requirements for Pathogenicity of Fusarium Oxysporum F. Sp. Lycopersici Through Large-Scale Insertional Mutagenesis
Genome Biology
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Type 2 Diabetes Locus on 12q15: Further Mapping and Mutation Screening of Two Candidate Genes
Diabetes
Internal Medicine
Endocrinology
Metabolism
Diabetes
Fine Mapping of Fatness QTL on Porcine Chromosome X and Analyses of Three Positional Candidate Genes
BMC Genetics
Genetics
Isolated Hereditary Congenital Facial Paralysis
The Differential Diagnosis of a Patient With Unilateral Congenital Facial Paralysis: 3q21 Deletion
Academic Journal of Pediatrics & Neonatology
Identification and Characterization of the TRIP8 and REEP3 Genes on Chromosome 10q21.3 as Novel Candidate Genes for Autism
European Journal of Human Genetics
Genetics
“Congenital Facial Palsy’’ - A Case Report and Literature Review”
Journal of Evolution of medical and Dental Sciences
A Novel Loss-Of-Function Mutation in HOXB1 Associated With Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family
Molecular Syndromology
Genetics
Refinement of Intraoral Reverse Temporalis Transfer for Facial Palsy Using a Mandibular Periosteum Flap
Archives of Plastic Surgery
Surgery
A Locus for Hereditary Sensory Neuropathy With Cough and Gastroesophageal Reflux on Chromosome 3p22-P24
American Journal of Human Genetics
Genetics