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Q55868116-46206F0B-6688-4664-A761-EB0F547DA949
Q55868116-46206F0B-6688-4664-A761-EB0F547DA949
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55868116-46206F0B-6688-4664-A761-EB0F547DA949
Further delineation of genotype-phenotype correlation in homozygous 2p21 deletion syndromes: first description of patients without cystinuria
P2860
Q55868116-46206F0B-6688-4664-A761-EB0F547DA949
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55868116-46206F0B-6688-4664-A761-EB0F547DA949
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Statement
wasDerivedFrom
ff157d41c003bc06d88d533bee0b85ea0a8b7da7
P2860
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.