Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders
Demars, Julie, Shmela, Mansur Ennuri, Rossignol, Sylvie, Okabe, Jun, Netchine, Irène, Azzi, Salah, Cabrol, Sylvie, Le Caignec, Cédric, David, Albert, Le Bouc, Yves, El-Osta, Assam, Gicquel, Christine
Published in Human molecular genetics (01.03.2010)
Published in Human molecular genetics (01.03.2010)
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Journal Article
Genetic variants within the second intron of the KCNQ1 gene affect CTCF binding and confer a risk of Beckwith–Wiedemann syndrome upon maternal transmission
Demars, Julie, Shmela, Mansur Ennuri, Khan, Abdul Waheed, Lee, Kai Syin, Azzi, Salah, Dehais, Patrice, Netchine, Irène, Rossignol, Sylvie, Le Bouc, Yves, El-Osta, Assam, Gicquel, Christine
Published in Journal of medical genetics (01.08.2014)
Published in Journal of medical genetics (01.08.2014)
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Journal Article
Genetic variants within the second intron of the KCNQ1 gene effect CTCF binding and confer a risk of Beckwith-Wiedemann syndrome upon maternal transmission
Demars, Julie, Shmela, Mansur Ennuri, Khan, Abdul Waheed, Lee, Kai Syin, Azzi, Salah, Dehais, Patrice, Netchine, Irène, Rossignol, Sylvie, Le Bouc, Yves, El Osta, Assam, Gicquel, C.
Published in Journal of medical genetics (2014)
Published in Journal of medical genetics (2014)
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Journal Article
Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11 p15 fetal growth disorders
DEMARS, Julie, ENNURI SHMELA, Mansur, EL-OSTA, Assam, GICQUEL, Christine, ROSSIGNOL, Sylvie, OKABE, Jun, NETCHINE, Irène, AZZI, Salah, CABROL, Sylvie, LE CAIGNEC, Cédric, DAVID, Albert, LE BOUC, Yves
Published in Human molecular genetics (2010)
Get full text
Published in Human molecular genetics (2010)
Journal Article