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Search Results - Clémantine, Dimartino
Search Results - Clémantine, Dimartino
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Generation of two induced pluripotent stem cell lines IMAGINi004-A and IMAGINi005-A from healthy donors
by
Quelennec, Eddy
,
Banal, Celine
,
Hamlin, Matthieu
,
Clémantine, Dimartino
,
Michael, Marie
,
Lefort, Nathalie
Published in
Stem cell research
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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis
by
Mak, Christopher C Y
,
Doherty, Dan
,
Lin, Angela E
,
Vegas, Nancy
,
Cho, Megan T
,
Viot, Géraldine
,
Dimartino, Clémantine
,
Weisfeld-Adams, James D
,
Lessel, Davor
,
Joss, Shelagh
,
Li, Chumei
,
Gonzaga-Jauregui, Claudia
,
Zarate, Yuri A
,
Ehmke, Nadja
,
Horn, Denise
,
Troyer, Caitlin
,
Kant, Sarina G
,
Lee, Youngha
,
Ishak, Gisele E
,
Leung, Gordon
,
Barone Pritchard, Amanda
,
Yang, Sandra
,
Bend, Eric G
,
Filippini, Francesca
,
Roadhouse, Chelsea
,
Lebrun, Nicolas
,
Mehaffey, Michele G
,
Martin, Pierre-Marie
,
Apple, Benjamin
,
Millan, Francisca
,
Puk, Oliver
,
Hoffer, Mariette J V
,
Henderson, Lindsay B
,
McGowan, Ruth
,
Wentzensen, Ingrid M
,
Pei, Steven
,
Zahir, Farah R
,
Yu, Mullin
,
Gibson, William T
,
Seman, Ann
,
Steeves, Marcie
,
Murrell, Jill R
,
Luettgen, Sabine
,
Francisco, Elizabeth
,
Strom, Tim M
,
Amlie-Wolf, Louise
,
Kaindl, Angela M
,
Wilson, William G
,
Halbach, Sara
,
Basel-Salmon, Lina
,
Lev-El, Noa
,
Denecke, Jonas
,
Vissers, Lisenka E L M
,
Radtke, Kelly
,
Chelly, Jamel
,
Zackai, Elaine
,
Friedman, Jan M
,
Bamshad, Michael J
,
Nickerson, Deborah A
,
Reid, Russell R
,
Devriendt, Koenraad
,
Chae, Jong-Hee
,
Stolerman, Elliot
,
McDougall, Carey
,
Powis, Zöe
,
Bienvenu, Thierry
,
Tan, Tiong Y
,
Orenstein, Naama
,
Dobyns, William B
,
Shieh, Joseph T
,
Choi, Murim
,
Waggoner, Darrel
,
Gripp, Karen W
,
Parker, Michael J
,
Stoler, Joan
,
Lyonnet, Stanislas
,
Cormier-Daire, Valérie
,
Viskochil, David
,
Hoffman, Trevor L
,
Amiel, Jeanne
,
Chung, Brian H Y
,
Gordon, Christopher T
Published in
Brain (London, England : 1878)
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A novel intronic variant in PIGB in Acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects
by
Palagano, Eleonora
,
Gordon, Christopher T.
,
Uva, Paolo
,
Strina, Dario
,
Dimartino, Clémantine
,
Villa, Anna
,
Amiel, Jeanne
,
Guion-Almeida, Maria L.
,
Vendramini-Pittoli, Siulan
,
Kokitsu-Nakata, Nancy M.
,
Zechi-Ceide, Roseli M.
,
Sobacchi, Cristina
Published in
Bone (New York, N.Y.)
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Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice
by
Martin, Ella M M A
,
Enriquez, Annabelle
,
Sparrow, Duncan B
,
Humphreys, David T
,
McInerney-Leo, Aideen M
,
Leo, Paul J
,
Duncan, Emma L
,
Iyer, Kavitha R
,
Greasby, Joelene A
,
Ip, Eddie
,
Giannoulatou, Eleni
,
Sheng, Delicia
,
Wohler, Elizabeth
,
Dimartino, Clémantine
,
Amiel, Jeanne
,
Capri, Yline
,
Lehalle, Daphné
,
Mory, Adi
,
Wilnai, Yael
,
Lebenthal, Yael
,
Gharavi, Ali G
,
Krzemień, Grażyna G
,
Miklaszewska, Monika
,
Steiner, Robert D
,
Raggio, Cathy
,
Blank, Robert
,
Baris Feldman, Hagit
,
Milo Rasouly, Hila
,
Sobreira, Nara L M
,
Jobling, Rebekah
,
Gordon, Christopher T
,
Giampietro, Philip F
,
Dunwoodie, Sally L
,
Chapman, Gavin
Published in
Human molecular genetics
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Correction to ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder
by
Carapito, Raphaël
,
Ivanova, Ekaterina
,
Morlon, Aurore
,
Meng, Linyan
,
Molitor, Anne
,
Erdmann, Eva
,
Kieffer, Bruno
,
Pichot, Angélique
,
Naegely, Lydie
,
Kolmer, Aline
,
Paul, Nicodème
,
Hanauer, Antoine
,
Tran Mau-Them, Frédéric
,
Jean-Marçais, Nolwenn
,
Hiatt, Susan
,
Cooper, Gregory
,
Tvrdik, Tatiana
,
Muir, Alison
,
Dimartino, Clémantine
,
Chopra, Maya
,
Amiel, Jeanne
,
Gordon, Christopher
,
Dutreux, Fabien
,
Garde, Aurore
,
Thauvin-Robinet, Christel
,
Wang, Xia
,
Leduc, Magalie
,
Phillips, Meredith
,
Crawford, Heather
,
Kukolich, Mary
,
Hunt, David
,
Harrison, Victoria
,
Kharbanda, Mira
,
Smigiel, Robert
,
Gold, Nina
,
Hung, Christina
,
Viskochil, David
,
Dugan, Sarah
,
Bayrak-Toydemir, Pinar
,
Joly-Helas, Géraldine
,
Guerrot, Anne-Marie
,
Schluth-Bolard, Caroline
,
Rio, Marlène
,
Wentzensen, Ingrid M.
,
Mcwalter, Kirsty
,
Schnur, Rhonda
,
Lewis, Andrea
,
Lalani, Seema
,
Mensah-Bonsu, Noël
,
Céraline, Jocelyn
,
Sun, Zijie
,
Ploski, Rafal
,
Bacino, Carlos
,
Mefford, Heather
,
Faivre, Laurence
,
Bodamer, Olaf
,
Chelly, Jamel
,
Isidor, Bertrand
,
Bahram, Seiamak
Published in
American journal of human genetics
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ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder
by
Carapito, Raphael
,
Ivanova, Ekaterina L.
,
Morlon, Aurore
,
Meng, Linyan
,
Molitor, Anne
,
Erdmann, Eva
,
Kieffer, Bruno
,
Pichot, Angélique
,
Naegely, Lydie
,
Kolmer, Aline
,
Paul, Nicodème
,
Hanauer, Antoine
,
Tran Mau-Them, Frédéric
,
Jean-Marçais, Nolwenn
,
Hiatt, Susan M.
,
Cooper, Gregory M.
,
Tvrdik, Tatiana
,
Muir, Alison M.
,
Dimartino, Clémantine
,
Chopra, Maya
,
Amiel, Jeanne
,
Gordon, Christopher T.
,
Dutreux, Fabien
,
Garde, Aurore
,
Thauvin-Robinet, Christel
,
Wang, Xia
,
Leduc, Magalie S.
,
Phillips, Meredith
,
Crawford, Heather P.
,
Kukolich, Mary K.
,
Hunt, David
,
Harrison, Victoria
,
Kharbanda, Mira
,
Smigiel, Robert
,
Gold, Nina
,
Hung, Christina Y.
,
Viskochil, David H.
,
Dugan, Sarah L.
,
Bayrak-Toydemir, Pinar
,
Joly-Helas, Géraldine
,
Guerrot, Anne-Marie
,
Schluth-Bolard, Caroline
,
Rio, Marlène
,
Wentzensen, Ingrid M.
,
McWalter, Kirsty
,
Schnur, Rhonda E.
,
Lewis, Andrea M.
,
Lalani, Seema R.
,
Mensah-Bonsu, Noël
,
Céraline, Jocelyn
,
Sun, Zijie
,
Ploski, Rafal
,
Bacino, Carlos A.
,
Mefford, Heather C.
,
Faivre, Laurence
,
Bodamer, Olaf
,
Chelly, Jamel
,
Isidor, Bertrand
,
Bahram, Seiamak
Published in
American journal of human genetics
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ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder
by
Carapito, Raphael
,
Ivanova, Ekaterina L.
,
Morlon, Aurore
,
Meng, Linyan
,
Molitor, Anne
,
Erdmann, Eva
,
Kieffer, Bruno
,
Pichot, Angélique
,
Naegely, Lydie
,
Kolmer, Aline
,
Paul, Nicodème
,
Hanauer, Antoine
,
Tran Mau-Them, Frédéric
,
Jean-Marçais, Nolwenn
,
Hiatt, Susan M.
,
Cooper, Gregory M.
,
Tvrdik, Tatiana
,
Muir, Alison M.
,
Dimartino, Clémantine
,
Chopra, Maya
,
Amiel, Jeanne
,
Gordon, Christopher T.
,
Dutreux, Fabien
,
Garde, Aurore
,
Thauvin-Robinet, Christel
,
Wang, Xia
,
Leduc, Magalie S.
,
Phillips, Meredith
,
Crawford, Heather P.
,
Kukolich, Mary K.
,
Hunt, David
,
Harrison, Victoria
,
Kharbanda, Mira
,
Smigiel, Robert
,
Gold, Nina
,
Hung, Christina Y.
,
Viskochil, David H.
,
Dugan, Sarah L.
,
Bayrak-Toydemir, Pinar
,
Joly-Helas, Géraldine
,
Guerrot, Anne-Marie
,
Schluth-Bolard, Caroline
,
Rio, Marlène
,
Wentzensen, Ingrid M.
,
McWalter, Kirsty
,
Schnur, Rhonda E.
,
Lewis, Andrea M.
,
Lalani, Seema R.
,
Mensah-Bonsu, Noël
,
Céraline, Jocelyn
,
Sun, Zijie
,
Ploski, Rafal
,
Bacino, Carlos A.
,
Mefford, Heather C.
,
Faivre, Laurence
,
Bodamer, Olaf
,
Chelly, Jamel
,
Isidor, Bertrand
,
Bahram, Seiamak
Published in
American journal of human genetics
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