Recognizable phenotype with common occurrence of microcephal…
Recognizable phenotype with common occurrence of microcephaly%2525252C psychomotor retardation%2525252C but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutations
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Wiley Online Library Database Model 2021
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- 2003~present
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Wiley Online Library: Complete Journals
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- 2003-01-01~present