Search Results - Wohlleber, Eva
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1
Phenotypic spectrum associated with CASK loss-of-function mutations by Moog, Ute (Author) , Kutsche, Kerstin (Author) , Kortüm, Fanny (Author) , Chilian, Bettina (Author) , Bierhals, Tatjana (Author) , Apeshiotis, Neophytos (Author) , Balg, Stefanie (Author) , Chassaing, Nicolas (Author) , Coubes, Christine (Author) , Das, Soma (Author) , Engels, Hartmut (Author) , Esch, Hilde Van (Author) , Grasshoff, Ute (Author) , Heise, Marisol (Author) , Isidor, Bertrand (Author) , Jarvis, Joanna (Author) , Koehler, Udo (Author) , Martin, Thomas (Author) , Oehl-Jaschkowitz, Barbara (Author) , Ortibus, Els (Author) , Pilz, Daniela T. (Author) , Prabhakar, Prab (Author) , Rappold, Gudrun (Author) , Rau, Isabella (Author) , Rettenberger, Günther (Author) , Schlüter, Gregor (Author) , Scott, Richard H. (Author) , Shoukier, Moonef (Author) , Wohlleber, Eva (Author) , Zirn, Birgit (Author) , Dobyns, William B. (Author) , Uyanik, Gökhan (Author) ,
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2
Phenotypic spectrum associated with CASK loss-of-function mutations by Moog, Ute (Author) , Kutsche, Kerstin (Author) , Kortüm, Fanny (Author) , Chilian, Bettina (Author) , Bierhals, Tatjana (Author) , Apeshiotis, Neophytos (Author) , Balg, Stefanie (Author) , Chassaing, Nicolas (Author) , Coubes, Christine (Author) , Das, Soma (Author) , Engels, Hartmut (Author) , Esch, Hilde Van (Author) , Grasshoff, Ute (Author) , Heise, Marisol (Author) , Isidor, Bertrand (Author) , Jarvis, Joanna (Author) , Koehler, Udo (Author) , Martin, Thomas (Author) , Oehl-Jaschkowitz, Barbara (Author) , Ortibus, Els (Author) , Pilz, Daniela T. (Author) , Prabhakar, Prab (Author) , Rappold, Gudrun (Author) , Rau, Isabella (Author) , Rettenberger, Günther (Author) , Schlüter, Gregor (Author) , Scott, Richard H. (Author) , Shoukier, Moonef (Author) , Wohlleber, Eva (Author) , Zirn, Birgit (Author) , Dobyns, William B. (Author) , Uyanik, Gökhan (Author) ,
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3
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits by Horn, Denise (Author) , Kapeller, Johannes (Author) , Rivera-Brugués, Núria (Author) , Moog, Ute (Author) , Lorenz-Depiereux, Bettina (Author) , Eck, Sebastian (Author) , Hempel, Maja (Author) , Wagenstaller, Janine (Author) , Gawthrope, Alex (Author) , Monaco, Anthony P. (Author) , Bonin, Michael (Author) , Riess, Olaf (Author) , Wohlleber, Eva (Author) , Illig, Thomas (Author) , Bezzina, Connie R. (Author) , Franke, Andre (Author) , Spranger, Stephanie (Author) , Villavicencio-Lorini, Pablo (Author) , Seifert, Wenke (Author) , Rosenfeld, Jochen (Author) , Klopocki, Eva (Author) , Rappold, Gudrun (Author) , Strom, Tim M. (Author) ,
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Related Subjects
CASK
FOXP1
X linked mental retardation
academic medicine
chromosomal
clinical genetics
copy number variations
copy-number
developmental, genetics
diagnostics
diagnostics tests
epigenetics
epilepsy and seizures
genetic screening/counselling
intellectual disability
language and speech deficits
mental retardation
microcephaly
molecular genetics
neurology
neurosciences, neurology
other neurology
pontocerebellar hypoplasia
visual development