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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 nor did they address autosomal-recessive and X-linked inheritance.
8 few recessive cases and a single instance of X-linked inheritance.
9 ified with autosomal dominant, recessive,and X-linked inheritance.
10 gene, is a complex and diverse disorder with X-linked inheritance.
11 rds males, which suggests the possibility of X-linked inheritance.
12 Of these families, 91 (39%) show definitive X-linked inheritance, an additional 88 (38%) reveal a pa
15 rotein (RP) genes while <1% of patients with X-linked inheritance have been identified with mutations
16 P497L) in the ubiquilin-2 gene (UBQLN2) with X-linked inheritance in all studied affected individuals
17 lation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX) is one of a group of clinica
19 Autosomal dominant, autosomal recessive and X-linked inheritance of disease-causing SVs were observe
20 ice, and rats that reflect its autosomal and X-linked inheritance patterns as well as different mutat
24 n geostatistical model adapted to the gene's X-linked inheritance, which predicted a G6PDd allele fre