9 results on '"Piard, Juliette"'
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2. Patient satisfaction, experience and preferences in the implementation of genetics teleconsultations in the North-eastern region of France
3. Split hand/foot malformation associated with 20p12.1 deletion: A case report
4. A new case of KIAA0753-related variant of Jeune asphyxiating thoracic dystrophy
5. Retards staturaux liés au gène SHOX : étude rétrospective multicentrique sur l’implication des CNVs et l’apport du séquençage
6. Autopsy findings of ectodermal dysplasia and sex development disorder in a fetus with 19q12q13 microdeletion
7. DYRK1A mutations in two unrelated patients
8. Coronal craniosynostosis and radial ray hypoplasia: A third report of Twist mutation in a 33 weeks fetus with diaphragmatic hernia
9. Systematic search for neutropenia should be part of the first screening in patients with poikiloderma
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