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Q33679891-54EDB4F0-1177-4755-9657-6514121C9B98
Q33679891-54EDB4F0-1177-4755-9657-6514121C9B98
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33679891-54EDB4F0-1177-4755-9657-6514121C9B98
Multiple congenital anomalies including the Rieger eye malformation in a boy with interstitial deletion of (4) (q25-->q27) secondary to a balanced insertion in his normal father: evidence for haplotype insufficiency causing the Rieger malformation.
P2860
Q33679891-54EDB4F0-1177-4755-9657-6514121C9B98
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33679891-54EDB4F0-1177-4755-9657-6514121C9B98
rank
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type
BestRank
Statement
wasDerivedFrom
aaa611547c88dc5f841645696fb82b2a52ba3226
P2860
Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193