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Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome
by
Ghedira, Nehla
,
Lagarde, Arnaud
,
Ben Ameur, Karim
,
Elouej, Sahar
,
Sakka, Rania
,
Kerkeni, Emna
,
Chioukh, Fatma-Zohra
,
Olschwang, Sylviane
,
Desvignes, Jean-Pierre
,
Abdelhak, Sonia
,
Delague, Valerie
,
Lévy, Nicolas
,
Monastiri, Kamel
,
De Sandre-Giovannoli, Annachiara
Published in
BMC pediatrics
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Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemia
by
Cavé, Hélène
,
Caye, Aurélie
,
Ghedira, Nehla
,
Capri, Yline
,
Pouvreau, Nathalie
,
Fillot, Natacha
,
Trimouille, Aurélien
,
Vignal, Cédric
,
Fenneteau, Odile
,
Alembik, Yves
,
Alessandri, Jean-Luc
,
Blanchet, Patricia
,
Boute, Odile
,
Bouvagnet, Patrice
,
David, Albert
,
Dieux Coeslier, Anne
,
Doray, Bérénice
,
Dulac, Olivier
,
Drouin-Garraud, Valérie
,
Gérard, Marion
,
Héron, Delphine
,
Isidor, Bertrand
,
Lacombe, Didier
,
Lyonnet, Stanislas
,
Perrin, Laurence
,
Rio, Marlène
,
Roume, Joëlle
,
Sauvion, Sylvie
,
Toutain, Annick
,
Vincent-Delorme, Catherine
,
Willems, Marjorie
,
Baumann, Clarisse
,
Verloes, Alain
Published in
European journal of human genetics : EJHG
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European Journal Of Human Genetics
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