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Search Results - Gross-Morand, Marie Sylvie
Search Results - Gross-Morand, Marie Sylvie
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Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia
by
Verkarre, V
,
Fournet, J C
,
de Lonlay, P
,
Gross-Morand, M S
,
Devillers, M
,
Rahier, J
,
Brunelle, F
,
Robert, J J
,
Nihoul-Fékété, C
,
Saudubray, J M
,
Junien, C
Published in
The Journal of clinical investigation
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Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pan...
by
de Lonlay, P
,
Fournet, J C
,
Rahier, J
,
Gross-Morand, M S
,
Poggi-Travert, F
,
Foussier, V
,
Bonnefont, J P
,
Brusset, M C
,
Brunelle, F
,
Robert, J J
,
Nihoul-Fékété, C
,
Saudubray, J M
,
Junien, C
Published in
The Journal of clinical investigation
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Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma
by
Blanquet, Véronique
,
Turleau, Catherine
,
Gross-Morand, Marie Sylvie
,
Sénamaud-Beaufort, Catherine
,
Doz, François
,
Besmond, Claude
Published in
Human molecular genetics
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cDNA cloning, tissue distribution and chromosomal localization of the human ID4 gene
by
Rigolet, M
,
Rich, T
,
Gross-Morand, M S
,
Molina-Gomes, D
,
Viegas-Pequignot, E
,
Junien, C
Published in
DNA research
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Journal Of Clinical Investigation
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Life Sciences & Biomedicine
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Base Sequence
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Beckwith-Wiedemann Syndrome
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Chromosomes, Human, Pair 11
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Hyperinsulinism - Genetics
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Loss Of Alleles
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