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Artikel
[x]
Original Investigation
[x]
Sacherschließung
Neurodevelopmental Disorders/genetics [MeSH]
(4)
Male [MeSH]
(4)
Mutation, Missense [MeSH]
(3)
Humans [MeSH]
(3)
Female [MeSH]
(3)
Phenotype [MeSH]
(2)
Pedigree [MeSH]
(2)
Nerve Tissue Proteins/genetics [MeSH]
(2)
Child, Preschool [MeSH]
(2)
Publikationstyp
Medium
Erscheinungsjahr
2024
(2)
2021
(2)
Institution
4 Treffer
Kurzansicht
E-Jahr
Zugriff
Typ
Operations
Further evidence of biallelic NAV3 variants associated with recessive neurodevelopmental disorder with dysmorphism, developmental delay, intellectual disability, and behavioral abnormalities
2024 .
Kakar, Naseebullah
|
Mascarenhas, Selinda
|
Ali, Asmat
|
Ijlal Haider, Syed M.
|
Badiger, Vaishnavi Ashok
|
Ghofrani, Mobina Shadman
|
Kruse, Nathalie
|
Hashmi, Sohana Nadeem
|
Pozojevic, Jelena
|
Balachandran, Saranya
|
Toft, Mathias
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Malik, Sajid
|
Händler, Kristian
|
Fatima, Ambrin
|
Iqbal, Zafar
|
Shukla, Anju
|
Spielmann, Malte
|
Radhakrishnan, Periyasamy
2024
http://purl.org/ontology/bibo/Article
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly
2024 .
Herbst, Charlotte
|
Bothe, Viktoria
|
Wegler, Meret
|
Axer-Schaefer, Susanne
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Audebert-Bellanger, Séverine
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Gecz, Jozef
|
Cogne, Benjamin
|
Feldman, Hagit Baris
|
Horn, Anselm H. C.
|
Hurst, Anna C. E.
|
Kelly, Melissa A.
|
Kruer, Michael C.
|
Kurolap, Alina
|
Laquerriere, Annie
|
Li, Megan
|
Mark, Paul R.
|
Morawski, Markus
|
Nizon, Mathilde
|
Pastinen, Tomi
|
Polster, Tilman
|
Saugier-Veber, Pascale
|
SeSong, Jang
|
Sticht, Heinrich
|
Stieler, Jens T.
|
Thifffault, Isabelle
|
van Eyk, Clare L.
|
Marcorelles, Pascale
|
Vezain-Mouchard, Myriam
|
Abou Jamra, Rami
|
Oppermann, Henry
2024
http://purl.org/ontology/bibo/Article
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy
2021 .
Parenti, Ilaria
|
Lehalle, Daphné
|
Nava, Caroline
|
Torti, Erin
|
Leitão, Elsa
|
Person, Richard
|
Mizuguchi, Takeshi
|
Matsumoto, Naomichi
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Kato, Mitsuhiro
|
Nakamura, Kazuyuki
|
de Man, Stella
|
Cope, Heidi
|
Shashi, Vandana
|
Friedman, Jennifer
|
Joset, Pascal
|
Steindl, Katharina
|
Rauch, Anita
|
Muffels, Irena
|
van Hasselt, Peter M
|
petit, florence
|
Smol, Thomas
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Le Guyader, Gwenaël
|
Bilan, Frédéric
|
Sorlin, Arthur
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Vitobello, Antonio
|
PHILIPPE, Christophe
|
van de Laar, Ingrid
|
van Slegtenhorst, Marjon A.
|
Campeau, Philippe
|
Au, Ping Yee
|
Nakashima, Mitsuko
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Saitsu, Hirotomo
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Yamamoto, Tatsuya
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Nomura, Yumiko
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Louie, Raymond
|
Lyons, Michael
|
Dobson, Amy
|
Plomp, Astrid S.
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Motazacker, M. Mahdi
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Kaiser, Frank J.
|
Timberlake, Andrew
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Fuchs, Sabine
|
Depienne, Christel
|
Mignot, Cyril
2021
http://purl.org/ontology/bibo/Article
Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males
2021 .
Kreienkamp, Hans-Jürgen
|
Wagner, Matias
|
Weigand, Heike
|
McConkie-Rossell, Allyn
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McDonald, Marie
|
Keren, Boris
|
Mignot, Cyril
|
Gauthier, Julie
|
Soucy, Jean-François
|
Michaud, Jacques L.
|
Dumas, Meghan
|
Smith, Rosemarie
|
Löbel, Ulrike
|
Hempel, Maja
|
Kubisch, Christian
|
Denecke, Jonas
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Campeau, Philippe M.
|
Bain, Jennifer M.
|
Lessel, Davor
2021
http://purl.org/ontology/bibo/Article