Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.
Idiopathic hypoparathyroidism has been reported to occur as an X-linked recessive disorder in two multigeneration kindreds. Affected individuals, who are males, suffer from infantile onset of epilepsy and hypocalcemia, which appears to be due to an isolated congenital defect of parathyroid gland dev...
Những tác giả chính: | Thakker, R, Davies, K, Whyte, M, Wooding, C, O'Riordan, J |
---|---|
Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
1990
|
Những quyển sách tương tự
-
MAPPING OF THE X-LINKED IDIOPATHIC HYPOPARATHYROID GENE TO XQ26-XQ27 BY LINKAGE STUDIES
Bằng: Thakker, R, et al.
Được phát hành: (1989) -
Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.
Bằng: Trump, D, et al.
Được phát hành: (1998) -
Genetic mapping studies of the X-linked recessive hypoparathyroid gene on the X chromosome (Xq27).
Bằng: Dixon, P, et al.
Được phát hành: (1996) -
Physical map of the Xq27 candidate region for X-linked recessive hypoparathyroidism in two kindreds merged by mitochondrial DNA analysis
Bằng: Mumm, S, et al.
Được phát hành: (1996) -
X-linked recessive hypoparathyroidism is caused by a molecular deletional-insertion involving chromosomes Xq27 and 2p25.
Bằng: Bowl, MR, et al.
Được phát hành: (2001)