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Nesbit M Andrew
Nesbit M Andrew
Biology
Genetics
Endocrinology
Internal medicine
Cancer research
4
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1
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0
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Sedlin mutations disrupt interactions with pituitary homeobox 1 (Pitx1) and steroidogenic factor 1 (SF1): potential cause of delayed puberty in boys with Spondyloepiphyseal dysplasia tarda (SEDT)
2007
Jeshmi Jeyabalan
Nesbit M Andrew
Holly A Ingraham
Rajesh V. Thakker
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Genome comparison between human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals loss, in man, of 5.1 Mb containing 4 mouse G-protein coupled receptors: relevance to familial benign hypocalciuric hypercalcaemia type 3
2007
Fadil Hannan
Nesbit M Andrew
Paul Christie
Brian Harding
Michael P. Whyte
Rajesh Thakker
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A novel homozygous inactivating mutation, Pro339Thr, of the calcium-sensing receptor is associated with isolated primary hyperparathyroidism
2007
Fadil Hannan
Nesbit M Andrew
Paul Christie
Willy Lissens
Marie Bex
Roger Bouillon
Rajesh Thakker
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Characterisation of parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) in 3 families with autosomal recessive hypoparathyroidism
2007
Michael R. Bowl
Samantha Mirczuk
Lorraine Southam
Zulf Mughal
Fiona Ryan
Nick Shaw
Elaine Tham
Zeev Hochberg
Dov Tiosano
John Loughlin
Nesbit M Andrew
Rajesh Thakker
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