Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-020-02147-1.pdf
Reference284 articles.
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3. Alatzoglou KS, Kelberman D, Cowell CT et al (2011) Increased transactivation associated with SOX3 polyalanine tract deletion in a patient with hypopituitarism. J Clin Endocrinol Metab. https://doi.org/10.1210/jc.2010-1239
4. Avilion AA, Nicolis SK, Pevny LH et al (2003) Multipotent cell lineages in early mouse development depend on SOX2 function. Genes Dev 17:126–140. https://doi.org/10.1101/gad.224503
5. Ayari B, Soussi-Yanicostas N (2007) FGFR1 and anosmin-1 underlying genetically distinct forms of Kallmann syndrome are co-expressed and interact in olfactory bulbs. Dev Genes Evol 217:169–175. https://doi.org/10.1007/s00427-006-0125-0
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