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#618019 - RHIZOMELIC SKELETAL DYSPLASIA WITH OR WITHOUT PELGER-HUET ANOMALY; SKPHA
Cytogenetic locations: 604903
Gene summaries Genetic tests Medical literature
#613471 - REYNOLDS SYNDROME
*600024 - LAMIN B RECEPTOR; LBR
#215140 - GREENBERG DYSPLASIA; GRBGD
#169400 - PELGER-HUET ANOMALY; PHA
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