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An intermediate phenotype in IDH related enchondromatosis spectrum
by
Yilmaz-Gulec, Elif
,
Marzin, Pauline
,
Huber-Lequesne, Céline
,
Cormier-Daire, Valérie
Published in
European journal of medical genetics
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Genotypes and Phenotypes of Children with SHOX Deficiency in France
by
Rosilio, Myriam
,
Huber-Lequesne, Céline
,
Sapin, Hélène
,
Carel, Jean-Claude
,
Blum, Werner F
,
Cormier-Daire, Valérie
Published in
The journal of clinical endocrinology and metabolism
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Síndrome 3-M: descripción clínica-radiológica: Caso clínico
by
Aracena A, Mariana
,
Macho F, Laura
,
Cornier-Daire, Valerie
,
Huber-Lequesne, Celine
,
Nishimura Y, Gen
Published in
Revista Chilena de pediatría
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European Journal Of Medical Genetics
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Revista Chilena De Pediatría
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The Journal Of Clinical Endocrinology And Metabolism
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Child
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Humans
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Life Sciences & Biomedicine
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Phenotype
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Science & Technology
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Adolescent
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Algorithms
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Body Height - Genetics
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Dna Mutational Analysis
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Dwarfism - Complications
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Dwarfism - Epidemiology
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Dwarfism - Genetics
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Enchondromatosis
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Enchondromatosis - Diagnostic Imaging
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Enchondromatosis - Genetics
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Endocrinology & Metabolism
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Female
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France - Epidemiology
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Genetic Association Studies
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