Recognizable phenotype with common occurrence of microcephal…
Recognizable phenotype with common occurrence of microcephaly%25252C psychomotor retardation%25252C but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutations
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- 2003~present; ;issue:1~present
Coverage:
- 2003-01-01~present; ;issue:1~present