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Commentary on “Megalencephaly-capillary malformation-polymicrogyria syndrome: the first case report in Korea”
Sung-Min Park, Byung-Soo Kim, Moon-Bum Kim, Hyun-Chang Ko
Clin Exp Pediatr. 2018;61(1):35-36.   Published online January 22, 2018
DOI: https://doi.org/10.3345/kjp.2018.61.1.35

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Commentary on “Megalencephaly-capillary malformation-polymicrogyria syndrome: the first case report in Korea”
Korean Journal of Pediatrics. 2018;61(1):35   Crossref logo
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Megalencephaly-capillary malformation-polymicrogyria syndrome: the first case report in Korea
Korean Journal of Pediatrics. 2016;59(Suppl 1):S152   Crossref logo
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The Orthopaedic Management of Hip Dysplasia with Underlying Megalencephaly-Capillary Malformation Syndrome: a Case Report
SN Comprehensive Clinical Medicine. 2022;4(1):   Crossref logo
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Expanding the differential diagnosis of fetal hydrops: an unusual prenatal presentation of megalencephaly-capillary malformation syndrome
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Megalencephaly–Capillary Malformation–Polymicrogyria with Cerebral Venous Thrombosis
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 2020;47(6):828-829   Crossref logo
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Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome
Journal of Child Neurology. 2012;28(5):651-657   Crossref logo
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Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria-polydactyly hydrocephalus syndromes
American Journal of Medical Genetics Part A. 2009;149A(5):868-876   Crossref logo
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Novel neonatal presentation of megalencephaly‐polymicrogyria‐pigmentary mosaicism syndrome (MPPM) related to MTOR mutation: Report of a case
Pediatric Dermatology. 2020;38(2):536-537   Crossref logo
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Gingival Biopsy to Detect Mosaicism in Overgrowth Syndromes: Report of Two Cases of Megalencephaly-Capillary Malformation Syndrome with Periodontal Anomalies
Case Reports in Dentistry. 2020;2020:1-5   Crossref logo
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eP097: The utility of CSF-derived cell free DNA in molecular diagnostics for the Megalencephaly-capillary Malformation (MCAP) syndrome: A case report
Genetics in Medicine. 2022;24(3):S63-S64   Crossref logo
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