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1 e also cause obesity and hormone resistance (pseudohypoparathyroidism).
2 ties of bone, as well as hormone resistance (pseudohypoparathyroidism caused by loss-of-function muta
3 type Ia (PHP-Ia) and in patients with pseudo-pseudohypoparathyroidism (pPHP).
4 lcemia in kindreds with PHP-Ia and/or pseudo-pseudohypoparathyroidism, two related disorders caused b
5  results in the hormone resistance syndrome, pseudohypoparathyroidism type 1a.
6 , results in the hormone-resistance syndrome pseudohypoparathyroidism type 1a.
7              Although the molecular basis of pseudohypoparathyroidism type 1b (PHP type 1b) remains u
8                                              Pseudohypoparathyroidism type 1B, a disorder of renal pa
9 protein (Gsalpha) are found in patients with pseudohypoparathyroidism type Ia (PHP-Ia) and in patient
10 has-deficient fibroblasts from patients with pseudohypoparathyroidism type Ia (PHP-Ia).
11  the alpha chain of G(s) (G alpha(s)) causes pseudohypoparathyroidism type Ia.
12 AS locus in humans causes autosomal dominant pseudohypoparathyroidism type Ib (AD-PHP-Ib(delNASm)), a
13 ed kindreds as a cause of autosomal dominant pseudohypoparathyroidism type Ib (AD-PHP-Ib).
14                                Patients with pseudohypoparathyroidism type Ib (PHP-Ib) have hypocalce
15                                              Pseudohypoparathyroidism type Ib (PHP-Ib) is a paternall
16  of inheritance is observed in kindreds with pseudohypoparathyroidism type Ib (PHP-Ib), which is most
17 ce are the only discernible abnormalities in pseudohypoparathyroidism type Ib (PHP-Ib).
18                                              Pseudohypoparathyroidism type IB (PHPIB) is associated w
19                                              Pseudohypoparathyroidism type IB (PHPIB) is characterize
20                   By contrast, subjects with pseudohypoparathyroidism type Ib have hormone resistance
21                      The molecular basis for pseudohypoparathyroidism type Ib is unknown.
22 des representing a murine autosomal-dominant pseudohypoparathyroidism type Ib model and one of only f
23  methylation imprints and autosomal-dominant pseudohypoparathyroidism type Ib, a disorder characteriz
24 rs and 15 additional unrelated subjects with pseudohypoparathyroidism type Ib.
25 mone resistance in these three brothers with pseudohypoparathyroidism type Ib.
26 amplify genomic DNA from three brothers with pseudohypoparathyroidism type Ib.
27 e imprinted GNAS cluster are associated with pseudohypoparathyroidism type Ib.
28 ) (L388R and E392K) that are associated with pseudohypoparathyroidism type Ic (PHPIc), a maternally i
29 S gene causes multiple phenotypes, including pseudohypoparathyroidism type-1B (PHP1B), a disorder of
30 ternal-specific exon 1A methylation leads to pseudohypoparathyroidism types 1A or 1B, respectively.