Géraldine Van Winckel

2PUBLICATIONS
16CO-AUTHORS
Epidemiological modellingAnthropological genetics
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Publications (2)

|Jan 11, 2024
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant.

Roberto Ricciardiello, Giulia Forleo, Lina Cipolla

|Jul 23, 2021
Homozygous GLI3 variants observed in three unrelated patients presenting with syndromic polydactyly.

Ahmed El Mouatani, Géraldine Van Winckel, Khaoula Zaafrane-Khachnaoui

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Frequent Collaborators

1 joint publications

Ahmed El Mouatani

1 joint publications

Khaoula Zaafrane-Khachnaoui

1 joint publications

Sandra Whalen

1 joint publications

Sophie Kaltenbach