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John Schulga
John Schulga
Forth Valley Royal Hospital
Medicine
Thyroid
Candidate gene
Trisomy
Congenital hypothyroidism
2
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0
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2024
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Peer Review of Paediatric Endocrine Services in the UK: A Template for Quality and Service Improvement.
2021
Hormone Research in Paediatrics
John Schulga
Heather Mitchell
S. Faisal Ahmed
Assunta Albanese
Justin T. Warner
Justin H. Davies
Nick Shaw
Indraneel Banerjee
Leena Patel
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A novel mutation in the PAX8 promoter region causes permanent congenital hypothyroidism in a patient with Down’s Syndrome
2014
Molecular and Cellular Pediatrics
Pia Hermanns
Sunia Khadouma
Scott Shepherd
Mohamed Mansor
John Schulga
Jez Jones
Malcolm Donaldson
Joachim Pohlenz
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