1 ties of bone, as well as hormone resistance (
pseudohypoparathyroidism caused by loss-of-function muta
2 type Ia (PHP-Ia) and in patients with pseudo-
pseudohypoparathyroidism (
pPHP).
3 lcemia in kindreds with PHP-Ia and/or pseudo-
pseudohypoparathyroidism,
two related disorders caused b
4 results in the hormone resistance syndrome,
pseudohypoparathyroidism type 1a.
5 , results in the hormone-resistance syndrome
pseudohypoparathyroidism type 1a.
6 Although the molecular basis of
pseudohypoparathyroidism type 1b (PHP type 1b) remains u
7 Pseudohypoparathyroidism type 1B, a disorder of renal pa
8 protein (Gsalpha) are found in patients with
pseudohypoparathyroidism type Ia (PHP-Ia) and in patient
9 has-deficient fibroblasts from patients with
pseudohypoparathyroidism type Ia (PHP-Ia).
10 the alpha chain of G(s) (G alpha(s)) causes
pseudohypoparathyroidism type Ia.
11 AS locus in humans causes autosomal dominant
pseudohypoparathyroidism type Ib (AD-PHP-Ib(delNASm)), a
12 ed kindreds as a cause of autosomal dominant
pseudohypoparathyroidism type Ib (AD-PHP-Ib).
13 Patients with
pseudohypoparathyroidism type Ib (PHP-Ib) have hypocalce
14 Pseudohypoparathyroidism type Ib (PHP-Ib) is a paternall
15 of inheritance is observed in kindreds with
pseudohypoparathyroidism type Ib (PHP-Ib), which is most
16 ce are the only discernible abnormalities in
pseudohypoparathyroidism type Ib (PHP-Ib).
17 Pseudohypoparathyroidism type IB (PHPIB) is associated w
18 Pseudohypoparathyroidism type IB (PHPIB) is characterize
19 By contrast, subjects with
pseudohypoparathyroidism type Ib have hormone resistance
20 The molecular basis for
pseudohypoparathyroidism type Ib is unknown.
21 des representing a murine autosomal-dominant
pseudohypoparathyroidism type Ib model and one of only f
22 methylation imprints and autosomal-dominant
pseudohypoparathyroidism type Ib, a disorder characteriz
23 rs and 15 additional unrelated subjects with
pseudohypoparathyroidism type Ib.
24 mone resistance in these three brothers with
pseudohypoparathyroidism type Ib.
25 amplify genomic DNA from three brothers with
pseudohypoparathyroidism type Ib.
26 e imprinted GNAS cluster are associated with
pseudohypoparathyroidism type Ib.
27 ternal-specific exon 1A methylation leads to
pseudohypoparathyroidism types 1A or 1B, respectively.