Suchergebnisse - "Keller, Kory"

PubPharm (37)

1

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

enthalten in: Genome medicine | 2021

von Gillentine, M. | Wang, T. | Hoekzema, K. | +98

2

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

enthalten in: Genome medicine | 2021

von Gillentine, M. | Wang, T. | Hoekzema, K. | +95

3

Autism and attention-deficit/hyperactivity disorders and symptoms in children with neurofibromatosis type 1

enthalten in: Developmental medicine and child neurology | 2021

von Morotti, H. | Mastel, S. | Keller, K. | +4

CommentIn: Dev Med Child Neurol. 2021 Feb;63(2):132. - PMID 32614454

4

Autism and attention‐deficit/hyperactivity disorders and symptoms in children with neurofibromatosis type 1

enthalten in: Developmental Medicine & Child Neurology | 2021

von Morotti, H. | Mastel, S. | Keller, K. | +4

5

Autism questionnaire scores do not only rise because of autism

enthalten in: Developmental Medicine & Child Neurology | 2021

von Fombonne, E. | Morotti, H. | Mastel, S. | +4

6

Autism questionnaire scores do not only rise because of autism

enthalten in: Developmental medicine and child neurology | 2021

von Fombonne, E. | Morotti, H. | Mastel, S. | +4

CommentOn: Dev Med Child Neurol. 2021 Feb;63(2):226-232. - PMID 32406525

7

The association of neurofibromatosis and autism symptomatology is confounded by behavioral problems

enthalten in: bioRxiv.org | 2020

von Morotti, H. | Mastel, S. | Keller, K. | +4

8

Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423 : genotype-phenotype study in neurofibromatosis type 1

enthalten in: Human mutation | 2020

von Koczkowska, M. | Callens, T. | Chen, Y. | +98

9

Clinical spectrum of individuals with pathogenic N F1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423 : genotype–phenotype study in neurofibromatosis type 1

enthalten in: Human mutation | 2020

von Koczkowska, M. | Callens, T. | Chen, Y. | +105

10

Two de novo novel mutations in one SHANK3 allele in a patient with autism and moderate intellectual disability

enthalten in: American journal of medical genetics. Part A | 2018

von Zhu, W. | Li, J. | Chen, S. | +11