P. Chenal

Exome sequencing identifies the first genetic determinants of sirenomelia in humans

C. V. van Ravenswaaij-Arts, T. Frebourg, S. Coutant, 2020, Human mutation.

Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system.

M. Gonzalès, M. Gubler, R. Bouvier, 2006, Journal of the American Society of Nephrology : JASN.

Tongue involvement revealing sarcoidosis.

I. Marie, H. Lévesque, A. Proux, 2008, QJM : monthly journal of the Association of Physicians.

Sirenomelia and caudal malformations in two families

B. Gérard, M. Gérard, V. Layet, 2012, American journal of medical genetics. Part A.

[Formaldehyde fixation in the third millennium].

E. Labouyrie, F. Plénat, J. Champigneulle, 2001, Annales de pathologie.

Reactive Eccrine Syringofibroadenomatosis Associated With Venous Leg Ulcers: A Case Report and Literature Review

P. Courville, P. Joly, C. Boulard, 2020, The international journal of lower extremity wounds.

[Drug-induced Sweet's syndrome related to hydroxychloroquine: About 2 cases].

C. Zarnitsky, N. Litrowski, C. Zarnitsky, 2019, La Revue de medecine interne.