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pro vyhledávání: '"Fouad Minkara"'
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Abstracts Accepted for Publication.
Background Monosomy 18p is a rare chromosomal disease resulting from complete or partial deletion of chromosome 18 short arm. It is associated with a variable phenotypic spectrum. Most reported patients have holoprosencephaly, developmental delay, sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e81b074420901232fbd34d7290538aa
https://doi.org/10.1136/annrheumdis-2019-eular.3774
https://doi.org/10.1136/annrheumdis-2019-eular.3774
