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Published in International journal of hygiene and environmental health (01.03.2019)
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Familial isolated congenital asplenia: a rare, frequently hereditary dominant condition, often detected too late as a cause of overwhelming pneumococcal sepsis. Report of a new case and review of 31 others
GILBERT, Brigitte, MENETREY, Céline, BELIN, Valérie, BROSSET, Philippe, DE LUMLEY, Lionel, FISHER, Alain
Published in European journal of pediatrics (01.07.2002)
Published in European journal of pediatrics (01.07.2002)
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SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
Cusin, Veronica, Viot, Géraldine, Munnich, Arnold, Toutain, Annick, Vekemans, Michel, Merrer, Martine Le, Girlich, Delphine, Cormier-Daire, Valérie, Belin, Valérie, Moncla, Anne
Published in Nature genetics (01.05.1998)
Published in Nature genetics (01.05.1998)
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Bilateral anophthalmia and oesophageal atresia in a newborn female: a new case of the anophthalmia-oesophageal-genital (AEG) syndrome
Menetrey, Céline, Belin, Valérie, Odent, Sylvie, de Lumley, Lionel, Gilbert, Brigitte
Published in Clinical dysmorphology (01.04.2002)
Published in Clinical dysmorphology (01.04.2002)
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