1  features in affected males, consistent with X-linked inheritance.

2 nction, polyendocrinopathy, enteropathy, and X-linked inheritance.

3 e transmission of the FOP phenotype excluded X-linked inheritance.

4 ccurs with autosomal dominant, recessive and X-linked inheritance.

5 f father-to-son transmission, thus excluding X-linked inheritance.

6 rome with this unusual phenotypic pattern of X-linked inheritance.

7 gene, is a complex and diverse disorder with X-linked inheritance.

8 rds males, which suggests the possibility of X-linked inheritance.

9  Of these families, 91 (39%) show definitive X-linked inheritance, an additional 88 (38%) reveal a pa

10                              As predicted by X-linked inheritance, female descendants of an affected

11                                              X-linked inheritance has important consequences for gene

12 rotein (RP) genes while <1% of patients with X-linked inheritance have been identified with mutations

13 P497L) in the ubiquilin-2 gene (UBQLN2) with X-linked inheritance in all studied affected individuals

14 lation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX) is one of a group of clinica

15 ulation, polyendocrinopathy, enteropathy and X-linked inheritance (MIM 304930).

16 autosomal dominant, autosomal recessive, and X-linked inheritance patterns have been described.

17                                              X-linked inheritance was confirmed by haplotype analysis

18 n geostatistical model adapted to the gene's X-linked inheritance, which predicted a G6PDd allele fre