In Response to: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies

Nienke van Engelen; Illja Diets; Dorine Bresters; Janneke C van den Bergen; Alexander F J E Vrancken; Roland P Kuiper; Marjolijn C J Jongmans

doi:10.1097/MPH.0000000000002373

In Response to: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies

Nienke van Engelen
, Illja Diets
, Dorine Bresters
, Janneke C van den Bergen
, Alexander F J E Vrancken
, Roland P Kuiper
, Marjolijn C J Jongmans

Group Kuiper

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

Original language	English
Pages (from-to)	69
Number of pages	1
Journal	Journal of pediatric hematology/oncology
Volume	44
Issue number	2
DOIs	https://doi.org/10.1097/MPH.0000000000002373
Publication status	Published - 1 Mar 2022

Keywords

Child
Germ Cells/metabolism
Germ-Line Mutation
Humans
Mutation
Myelodysplastic Syndromes/genetics
Noonan Syndrome
Phenotype
ras Proteins/genetics

Access to Document

10.1097/MPH.0000000000002373

Cite this

van Engelen, N., Diets, I., Bresters, D., van den Bergen, J. C., Vrancken, A. F. J. E., Kuiper, R. P., & Jongmans, M. C. J. (2022). In Response to: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies. Journal of pediatric hematology/oncology, 44(2), 69. https://doi.org/10.1097/MPH.0000000000002373

@article{f4b0f050f3f74d59b0e786ffa2de3f53,

title = "In Response to: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies",

keywords = "Child, Germ Cells/metabolism, Germ-Line Mutation, Humans, Mutation, Myelodysplastic Syndromes/genetics, Noonan Syndrome, Phenotype, ras Proteins/genetics",

author = "\{van Engelen\}, Nienke and Illja Diets and Dorine Bresters and \{van den Bergen\}, \{Janneke C\} and Vrancken, \{Alexander F J E\} and Kuiper, \{Roland P\} and Jongmans, \{Marjolijn C J\}",

year = "2022",

month = mar,

day = "1",

doi = "10.1097/MPH.0000000000002373",

language = "English",

volume = "44",

pages = "69",

journal = "Journal of pediatric hematology/oncology",

issn = "1077-4114",

publisher = "Lippincott Williams and Wilkins",

number = "2",

}

van Engelen, N, Diets, I, Bresters, D, van den Bergen, JC, Vrancken, AFJE, Kuiper, RP & Jongmans, MCJ 2022, 'In Response to: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies', Journal of pediatric hematology/oncology, vol. 44, no. 2, pp. 69. https://doi.org/10.1097/MPH.0000000000002373

In Response to: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies. / van Engelen, Nienke; Diets, Illja; Bresters, Dorine et al.
In: Journal of pediatric hematology/oncology, Vol. 44, No. 2, 01.03.2022, p. 69.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - In Response to: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies

T2 - Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies

AU - van Engelen, Nienke

AU - Diets, Illja

AU - Bresters, Dorine

AU - van den Bergen, Janneke C

AU - Vrancken, Alexander F J E

AU - Kuiper, Roland P

AU - Jongmans, Marjolijn C J

PY - 2022/3/1

Y1 - 2022/3/1

KW - Child

KW - Germ Cells/metabolism

KW - Germ-Line Mutation

KW - Humans

KW - Mutation

KW - Myelodysplastic Syndromes/genetics

KW - Noonan Syndrome

KW - Phenotype

KW - ras Proteins/genetics

UR - https://www.scopus.com/pages/publications/85125290296

U2 - 10.1097/MPH.0000000000002373

DO - 10.1097/MPH.0000000000002373

M3 - Article

C2 - 34935735

SN - 1077-4114

VL - 44

SP - 69

JO - Journal of pediatric hematology/oncology

JF - Journal of pediatric hematology/oncology

IS - 2

ER -

van Engelen N, Diets I, Bresters D, van den Bergen JC, Vrancken AFJE, Kuiper RP et al. In Response to: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies. Journal of pediatric hematology/oncology. 2022 Mar 1;44(2):69. doi: 10.1097/MPH.0000000000002373