Zoekresultaten - Vimal Maheshwari
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A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype door Deepa Banker, Bhavdeep Mungala, Zankhana Parekh, Shachi Ganatra, Vimal Maheshwari, Yashica Raj, Utsav Patel, Digant Patel, Kishan Chamar, Vasu Solanki
Gepubliceerd in 2023Plaatsingsnummer: Wordt geladen…Connect to this object online.
Locatie: Wordt geladen…
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