genetic defect in thyroid hormonogenesis ii b

genetic defect in thyroid hormonogenesis ii b - also known as or related to pendred's syndrome, pendreds syndrome, thyroid hormone organification defect ii b, hypothyroidism with sensorineural deafness, gdth iib, goitre-deafness syndrome
Key
Information LeafletsInformation Leaflet Support GroupsSupport Groups Patient PlusPatientPlus Medicine InfoMedicine Info
Pharmacy ProductsPharmacy Products Selected UK WebsitesSelected UK Websites Patient ExperiencePatient Experience BookBook
GuidelinesGuideline VideosVideos DiagramDiagram Medical EquipmentMedical Equipment

You searched for 'genetic defect in thyroid hormonogenesis ii b'

We found 1 resources matching on 'GENETIC DEFECT IN THYROID HORMONOGENESIS II B'

Show the top results
PatientPlusHypothyroidism     Print (html) this document
1 resource found for 'GENETIC DEFECT IN THYROID HORMONOGENESIS II B'
Other useful resources
Selected UK WebsitesBenefits / Grants / Financial Help     Print (html) this document
Find a doctor, hospital, dentist, therapist, etc Find a doctor, hospital, dentist, therapist, etc      
Choices when you are referred to a specialistChoices When Referred to a Specialist      
Create an online visiting room for a loved one in hospitalCreate an online visiting room for a loved one in hospital