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Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences: relevance to familial benign hypocalciuric hypercalcaemia type 3.
Eur J Hum Genet. 2010 Apr;18(4):442-7. doi: 10.1038/ejhg.2009.161. Epub 2009 Oct 7.
Eur J Hum Genet. 2010.
PMID: 19809483
Free PMC article.
Novel intronic mutation of MEN1 gene causing familial isolated primary hyperparathyroidism.
Carrasco CA, González AA, Carvajal CA, Campusano C, Oestreicher E, Arteaga E, Wohllk N, Fardella CE.
Carrasco CA, et al.
J Clin Endocrinol Metab. 2004 Aug;89(8):4124-9. doi: 10.1210/jc.2003-032101.
J Clin Endocrinol Metab. 2004.
PMID: 15292357
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