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#615656 - CHROMOSOME 15q11.2 DELETION SYNDROME
Gene summaries Genetic tests Medical literature
#612281 - ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6; ARCI6
Cytogenetic locations: Igtp
*609383 - NIPA-LIKE DOMAIN-CONTAINING PROTEIN 4; NIPAL4
Cytogenetic locations: #>#Q##
*608147 - TUBULIN-GAMMA COMPLEX-ASSOCIATED PROTEIN 5; TUBGCP5
Cytogenetic locations: mutation
*608146 - NIPA MAGNESIUM TRANSPORTER 2; NIPA2
*608145 - NIPA MAGNESIUM TRANSPORTER 1; NIPA1
*606322 - CYTOPLASMIC FMRP-INTERACTING PROTEIN 1; CYFIP1
#600363 - SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6
Cytogenetic locations: p##m##
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