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Recognizable phenotype with common occurrence of microcephal…
Recognizable phenotype with common occurrence of microcephaly%2C psychomotor retardation%2C but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutations
Recognizable phenotype with common occurrence of microcephaly%2C psychomotor retardation%2C but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutations
Article, Chapter
Authors: D. Kouwenberg
Publication: American Journal of Medical Genetics Part A, Volume:155A, Issue:9
Published: Wiley, 2011
ISSN: 1552-4825
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