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Longer titles found: Waardenburg syndrome type 1 (view), Waardenburg syndrome type 2D (view), Waardenburg syndrome type 4A (view)

searching for Waardenburg syndrome 8 found (98 total)

alternate case: waardenburg syndrome

Waardenburg anophthalmia syndrome (471 words) [view diff] no match in snippet view article find links to article

Waardenburg anophthalmia syndrome is a rare autosomal recessive genetic disorder which is characterized by either microphthalmia or anophthalmia, osseous

Congenital hearing loss (1,236 words) [view diff] case mismatch in snippet view article find links to article

dominant congenital hearing loss can be attributed to such causes like Waardenburg Syndrome. In autosomal recessive hearing loss, both parents who typically

List of diseases (A) (1,929 words) [view diff] exact match in snippet view article

Anophthalmia plus syndrome Anophthalmia short stature obesity Anophthalmia Waardenburg syndrome Anophthalmos Anophthalmos, clinical Anophthalmos with limb anomalies

List of abbreviations for diseases and disorders (112 words) [view diff] exact match in snippet view article find links to article

genitourinary anomalies, and mental retardation syndrome WD Wilson's disease WEE Western equine encephalitis WS Williams syndrome WS4 Waardenburg syndrome type 4

Examples of in vitro transdifferentiation by lineage-instructive approach (1,129 words) [view diff] exact match in snippet view article find links to article

S. A.; Miki, T. (1996). "Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics"

FAM227a (1,041 words) [view diff] exact match in snippet view article find links to article

L., Eric, V., & Fabiola, Q. R. (2014). Phenotypic variability in Waardenburg syndrome resulting from a 22q12. 3‐q13. 1 microdeletion involving SOX10. American

CCDC138 (1,124 words) [view diff] case mismatch in snippet view article find links to article

domain protein, expressed in embryogenesis, mutations correlate to Waardenburg Syndrome Embryonic structures, muscle, skeletal, muscles ZF5 POZ domain zinc

Dandy–Walker malformation (5,483 words) [view diff] exact match in snippet view article find links to article

Rubinstein–Taybi syndrome, Marden–Walker syndrome, Sheldon–Hall syndrome, Shah–Waardenburg syndrome, Fryns syndrome, Walker–Warburg syndrome, Fukuyama congenital muscular