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Author/Creator Boudry‐Labis, Elise

1. Diagnosis of intrachromosomal amplification of chromosome 21 (iAMP21) by molecular cytogenetics in pediatric acute lymphoblastic leukemia. Issue 10 (26th August 2015)

Authors:
Duployez, Nicolas; Boudry‐Labis, Elise; Decool, Gauthier; Grzych, Guillaume; Grardel, Nathalie; Abou Chahla, Wadih; Preudhomme, Claude; Roche‐Lestienne, Catherine
Journal:
Clinical case reports
Issue:
Volume 3:Issue 10(2015:Oct.)
Page Start:
814
Record Type:
Journal Article
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2. Dissection of contiguous gene effects for deletions around ERF on chromosome 19. Issue 7 (16th May 2021)

Authors:
Calpena, Eduardo; McGowan, Simon J.; Blanco Kelly, Fiona; Boudry‐Labis, Elise; Dieux‐Coeslier, Anne; Harrison, Rachel; Johnson, Diana; Lachlan, Katherine; Morton, Jenny E. V.; Stewart, Helen; Vasudevan, Pradeep; Twigg, Stephen R. F.; Wilkie, Andrew O. M.
Journal:
Human mutation
Issue:
Volume 42:Issue 7(2021)
Page Start:
811
Record Type:
Journal Article
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3. Neurofibromatosis‐1 gene deletions and mutations in de novo adult acute myeloid leukemia. Issue 4 (5th March 2013)

Authors:
Boudry‐Labis, Elise; Roche‐Lestienne, Catherine; Nibourel, Olivier; Boissel, Nicolas; Terre, Christine; Perot, Christine; Eclache, Virginie; Gachard, Nathalie; Tigaud, Isabelle; Plessis, Ghislaine; Cuccuini, Wendy; Geffroy, Sandrine; Villenet, Céline; Figeac, Martin; Leprêtre, Frederic; Rennevill...
Journal:
American journal of hematology
Issue:
Volume 88:Issue 4(2013:Apr.)
Page Start:
306
Record Type:
Journal Article
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4. WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion. Issue 6 (11th April 2017)

Authors:
Huynh, Minh Tuan; Boudry‐Labis, Elise; Duban, Bénédicte; Andrieux, Joris; Tran, Cong Toai; Tampere, Heidi; Ceraso, Delphine; Manouvrier, Sylvie; Tachdjian, Gérard; Roche‐Lestienne, Catherine; Vincent‐Delorme, Catherine
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 6(2017)
Page Start:
1690
Record Type:
Journal Article
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