Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Prashant Sanjay Jagtap"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 4, Pp GD01-GD03 (2021)
Pentasomy X is a rare syndrome with variable phenotype, that affects females with characteristic clinical features such as severe mental retardation with delayed speech, short stature, facial dimorphism, osseous, articular/skeletal/limb abnormalitie
Externí odkaz:
https://doaj.org/article/ad536c243c9b45efb9cbba59b6f40af8
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 4, Pp GD01-GD03 (2021)
Pentasomy X is a rare syndrome with variable phenotype, that affects females with characteristic clinical features such as severe mental retardation with delayed speech, short stature, facial dimorphism’s, osseous, articular/skeletal/limb abnormali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d626a71c593479f7765f927d68fcf319
https://doi.org/10.7860/jcdr/2021/46365.14752
https://doi.org/10.7860/jcdr/2021/46365.14752