Novel gross deletion at the LHX4 gene locus in a child with growth hormone deficiency
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference24 articles.
1. A mutation in the POU-Homeodomain of Pit-1 responsible for combined pituitary hormone deficiency;Radovick;Science.,1992
2. A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism;Castinetti;J. Clin. Endocrinol. Metab.,2008
3. Syndromic short stature in patients with a Germline mutation in the LIM Homeobox LHX4;Machinis;Am. J. Hum. Genet.,2001
4. Genetic regulation of pituitary gland development in human and mouse;Kelberman;Endocr. Rev.,2009
5. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia;Mitelman;Nat. Genet.,1997
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