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searching for Opitz G/BBB syndrome 5 found (14 total)

alternate case: opitz G/BBB syndrome

DiGeorge syndrome (5,275 words) [view diff] no match in snippet view article find links to article

DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22. While the symptoms
Trisomy 22 (739 words) [view diff] exact match in snippet view article find links to article
syndrome, DiGeorge syndrome, conotruncal anomaly face syndrome, Opitz G/BBB syndrome, and Cayler cardiofacial syndrome. The effects of this disorder are
Widow's peak (1,340 words) [view diff] exact match in snippet view article find links to article
and Aarskog syndrome. Widow's Peaks are also seen to derive from Opitz G/BBB syndrome. Widow's peaks are slightly more common among males, although in
List of abbreviations for diseases and disorders (112 words) [view diff] exact match in snippet view article find links to article
ectodermal dysplasia XLMTM X-linked myotubular myopathy XLOS X-linked Opitz G/BBB syndrome XLP syndrome X-linked lymphoproliferative syndrome (see Duncan Disease)
Craniofacial cleft (3,571 words) [view diff] exact match in snippet view article find links to article
coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome. J. Med. Genet. 52, 104–110. Wilcox, A. J; Lie, R. T.; Solvoll, K