The development of the mammalian outer and middle ear

Congenital aural atresia associated with agenesis of internal carotid artery in a girl with aFOXI3deletion

(2015) Elisa Tassano et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Effect of otitis media with effusion and its clinical intervention on the development of mastoid in children

(2014) Nina Chen et al.   ACTA OTO-LARYNGOLOGICA

The canine jaw-ear connection: The malleomandibular and tympanomandibular ligaments

(2014) Cathryn Stevens-Sparks et al.   Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology

Foxi transcription factors promote pharyngeal arch development by regulating formation of FGF signaling centers

(2014) Renée K. Edlund et al.   DEVELOPMENTAL BIOLOGY

A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome

(2014) Jennifer C. Fuchs et al.   HUMAN MOLECULAR GENETICS

FGF23 Deficiency Leads to Mixed Hearing Loss and Middle Ear Malformation in Mice

(2014) Andrew C. Lysaght et al.   PLoS One

SAMS, a Syndrome of Short Stature, Auditory-Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Is a Unique Neurocristopathy Caused by Mutations in Goosecoid

(2013) David A. Parry et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mouse Hoxa2 mutations provide a model for microtia and auricle duplication

(2013) M. Minoux et al.   DEVELOPMENT

HOXA2Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss

(2013) Kerry K. Brown et al.   HUMAN MUTATION

Observation of Apoptosis and Bone Lamella Structures in the Human Mastoid

(2013) Daisuke Fujiyama et al.   OTOLOGY & NEUROTOLOGY

Dual Origin of the Epithelium of the Mammalian Middle Ear

(2013) H. Thompson et al.   SCIENCE

Interaction between Foxc1 and Fgf8 during Mammalian Jaw Patterning and in the Pathogenesis of Syngnathia

(2013) Kimberly E. Inman et al.   PLoS Genetics

Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure

(2012) Charlotte L Bendon et al.   BMC Medical Genetics

The origin of the stapes and relationship to the otic capsule and oval window

(2012) Hannah Thompson et al.   DEVELOPMENTAL DYNAMICS

Of mice, moles and guinea pigs: Functional morphology of the middle ear in living mammals

(2012) Matthew J. Mason   HEARING RESEARCH

Evolution of the mammalian middle ear and jaw: adaptations and novel structures

(2012) Neal Anthwal et al.   JOURNAL OF ANATOMY

Development and homeostasis of the sebaceous gland

(2012) Catherin Niemann et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

New insights into mechanism of Eustachian tube ventilation based on cine computed tomography images

(2011) Michael H. McDonald et al.   EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY

A comprehensive review of reported heritable noggin-associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term: NOG-related-symphalangism spectrum disorder (NOG-SSD)

(2011) Tommy A. Potti et al.   HUMAN MUTATION

Scleraxis is Required for Differentiation of the Stapedius and Tensor Tympani Tendons of the Middle Ear

(2011) Lingyan Wang et al.   JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY

A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice

(2011) Jennifer A. Calvert et al.   MAMMALIAN GENOME

The Prevalence of Tympanic Membrane and Related Middle Ear Pathology in Children

(2011) A. Richard Maw et al.   OTOLOGY & NEUROTOLOGY

Defects in middle ear cavitation cause conductive hearing loss in the Tcof1 mutant mouse

(2010) Carol A. Richter et al.   HUMAN MOLECULAR GENETICS

Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass

(2009) Robert J Munroe et al.   BMC DEVELOPMENTAL BIOLOGY

Age- and sex-related changes in the normal human ear

(2009) Chiarella Sforza et al.   FORENSIC SCIENCE INTERNATIONAL

Development of the stapedius muscle and pyramidal eminence in humans

(2009) J. F. Rodríguez-Vázquez   JOURNAL OF ANATOMY

Genetics of microtia and associated syndromes

(2009) F Alasti et al.   JOURNAL OF MEDICAL GENETICS

A robust and high-throughput Cre reporting and characterization system for the whole mouse brain

(2009) Linda Madisen et al.   NATURE NEUROSCIENCE

Genetics of Otosclerosis

(2009) Melissa Thys et al.   OTOLOGY & NEUROTOLOGY

Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome

(2008) Daniel F. Schorderet et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

(2008) Fatemeh Alasti et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Metabolic mode peculiar to Meckels cartilage: immunohistochemical comparisons of hypoxia-inducible factor-1 and glucose transporters in developing endochondral bones in mice

(2008) Yasunori Sakakura et al.   EUROPEAN JOURNAL OF ORAL SCIENCES