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Helicobacter
The idiotypes of V kappa 21 light chains.
An Alu-mediated rearrangement causing a 3.2kb deletion and a novel two base pair deletion in AAAS gene as the cause of triple A syndrome.
Excluding Male Trainees in Obstetrics and Gynecology: Why We Do It and Why It's Wrong.
Mutations in the NKX2.5 gene and the PAX8 promoter in a girl with thyroid dysgenesis.
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Mutations in the NKX2.5 gene and the PAX8 promoter in a girl with thyroid dysgenesis.
Mutations in the NKX2.5 gene and the PAX8 promoter in a girl with thyroid dysgenesis. J Clin Endocrinol Metab. 2011 Jun; 96(6):E977-81.
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PubMed
subject areas
Congenital Hypothyroidism
Female
Homeobox Protein Nkx-2.5
Homeodomain Proteins
Humans
Mutation
Paired Box Transcription Factors
PAX8 Transcription Factor
Promoter Regions, Genetic
Thyroid Dysgenesis
Transcription Factors
authors with profiles
Samuel Refetoff