Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 9

1.

Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.

Koh JW, Kang SY, Kim GH, Yoo HW, Yu J.

Ann Pediatr Endocrinol Metab. 2013 Jun;18(2):90-4. doi: 10.6065/apem.2013.18.2.90. Epub 2013 Jun 30.

2.

Primary adrenal insufficiency caused by a novel mutation in DAX1 gene.

Evliyaoğlu O, Dokurel İ, Bucak F, Özcabı B, Ercan Ö, Ceylaner S.

J Clin Res Pediatr Endocrinol. 2013;5(1):55-7. doi: 10.4274/Jcrpe.895.

3.
4.

Evidence of adrenal failure in aging Dax1-deficient mice.

Scheys JO, Heaton JH, Hammer GD.

Endocrinology. 2011 Sep;152(9):3430-9. doi: 10.1210/en.2010-0986. Epub 2011 Jul 5.

5.

Hypogonadotropic hypogonadism in subjects with DAX1 mutations.

Jadhav U, Harris RM, Jameson JL.

Mol Cell Endocrinol. 2011 Oct 22;346(1-2):65-73. doi: 10.1016/j.mce.2011.04.017. Epub 2011 Jun 13. Review.

6.

DAX1 mutations map to putative structural domains in a deduced three-dimensional model.

Zhang YH, Guo W, Wagner RL, Huang BL, McCabe L, Vilain E, Burris TP, Anyane-Yeboa K, Burghes AH, Chitayat D, Chudley AE, Genel M, Gertner JM, Klingensmith GJ, Levine SN, Nakamoto J, New MI, Pagon RA, Pappas JG, Quigley CA, Rosenthal IM, Baxter JD, Fletterick RJ, McCabe ER.

Am J Hum Genet. 1998 Apr;62(4):855-64.

7.
8.

Clinical presentation, growth, and pubertal development in Addison's disease.

Grant DB, Barnes ND, Moncrieff MW, Savage MO.

Arch Dis Child. 1985 Oct;60(10):925-8.

9.

Recently recognized chromosomal defects of clinical importance.

Pembrey M, Baraitser M.

Postgrad Med J. 1986 Feb;62(724):131-42. Review.

Supplemental Content

Support Center