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Q53059336-AED92695-1660-457E-8715-97D0F1CD4F72
Q53059336-AED92695-1660-457E-8715-97D0F1CD4F72
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53059336-AED92695-1660-457E-8715-97D0F1CD4F72
Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion.
P2860
Q53059336-AED92695-1660-457E-8715-97D0F1CD4F72
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53059336-AED92695-1660-457E-8715-97D0F1CD4F72
rank
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Statement
wasDerivedFrom
7df30b333e4c9b532a7afb16908885b2b8a9efa7
P2860
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.