RAC1 Missense Mutations in Developmental Disorders with Diverse PhenotypesCitation formats

  • External authors:
  • Margot Reijners
  • Nurhuda Mohamad Ansor
  • Maria Kousi
  • Wyatt Yue
  • Perciliz Tan
  • Katie Clarkson
  • Ken Corning
  • Julie Jones
  • Wayne Lam
  • Grazia Mancini
  • Carlo Marcelis
  • Shehla Mohammed
  • Rolph Pfundt
  • Maian Roifman
  • Ronald Cohn
  • David Chiayat
  • Nicholas Katsanis
  • Han Brunner

Standard

RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. / Reijners, Margot; Mohamad Ansor, Nurhuda; Kousi, Maria; Yue, Wyatt; Tan, Perciliz; Clarkson, Katie; Clayton-Smith, Jill; Corning, Ken; Jones, Julie; Lam, Wayne; Mancini, Grazia; Marcelis, Carlo; Mohammed, Shehla; Pfundt, Rolph; Roifman, Maian; Cohn, Ronald; Chiayat, David; Millard, Thomas; Katsanis, Nicholas; Brunner, Han; Banka, Siddharth.

In: American Journal of Human Genetics, Vol. 101, No. 3, 2017, p. 466-477.

Research output: Contribution to journalArticlepeer-review

Harvard

Reijners, M, Mohamad Ansor, N, Kousi, M, Yue, W, Tan, P, Clarkson, K, Clayton-Smith, J, Corning, K, Jones, J, Lam, W, Mancini, G, Marcelis, C, Mohammed, S, Pfundt, R, Roifman, M, Cohn, R, Chiayat, D, Millard, T, Katsanis, N, Brunner, H & Banka, S 2017, 'RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes', American Journal of Human Genetics, vol. 101, no. 3, pp. 466-477. https://doi.org/10.1016/j.ajhg.2017.08.007

APA

Reijners, M., Mohamad Ansor, N., Kousi, M., Yue, W., Tan, P., Clarkson, K., Clayton-Smith, J., Corning, K., Jones, J., Lam, W., Mancini, G., Marcelis, C., Mohammed, S., Pfundt, R., Roifman, M., Cohn, R., Chiayat, D., Millard, T., Katsanis, N., ... Banka, S. (2017). RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. American Journal of Human Genetics, 101(3), 466-477. https://doi.org/10.1016/j.ajhg.2017.08.007

Vancouver

Reijners M, Mohamad Ansor N, Kousi M, Yue W, Tan P, Clarkson K et al. RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. American Journal of Human Genetics. 2017;101(3):466-477. https://doi.org/10.1016/j.ajhg.2017.08.007

Author

Reijners, Margot ; Mohamad Ansor, Nurhuda ; Kousi, Maria ; Yue, Wyatt ; Tan, Perciliz ; Clarkson, Katie ; Clayton-Smith, Jill ; Corning, Ken ; Jones, Julie ; Lam, Wayne ; Mancini, Grazia ; Marcelis, Carlo ; Mohammed, Shehla ; Pfundt, Rolph ; Roifman, Maian ; Cohn, Ronald ; Chiayat, David ; Millard, Thomas ; Katsanis, Nicholas ; Brunner, Han ; Banka, Siddharth. / RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. In: American Journal of Human Genetics. 2017 ; Vol. 101, No. 3. pp. 466-477.

Bibtex

@article{6d6a69481ce146c986953aa783ea3ff6,
title = "RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes",
author = "Margot Reijners and {Mohamad Ansor}, Nurhuda and Maria Kousi and Wyatt Yue and Perciliz Tan and Katie Clarkson and Jill Clayton-Smith and Ken Corning and Julie Jones and Wayne Lam and Grazia Mancini and Carlo Marcelis and Shehla Mohammed and Rolph Pfundt and Maian Roifman and Ronald Cohn and David Chiayat and Thomas Millard and Nicholas Katsanis and Han Brunner and Siddharth Banka",
year = "2017",
doi = "10.1016/j.ajhg.2017.08.007",
language = "English",
volume = "101",
pages = "466--477",
journal = "American Journal of Human Genetics",
issn = "0002-9297",
publisher = "Cell Press",
number = "3",

}

RIS

TY - JOUR

T1 - RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes

AU - Reijners, Margot

AU - Mohamad Ansor, Nurhuda

AU - Kousi, Maria

AU - Yue, Wyatt

AU - Tan, Perciliz

AU - Clarkson, Katie

AU - Clayton-Smith, Jill

AU - Corning, Ken

AU - Jones, Julie

AU - Lam, Wayne

AU - Mancini, Grazia

AU - Marcelis, Carlo

AU - Mohammed, Shehla

AU - Pfundt, Rolph

AU - Roifman, Maian

AU - Cohn, Ronald

AU - Chiayat, David

AU - Millard, Thomas

AU - Katsanis, Nicholas

AU - Brunner, Han

AU - Banka, Siddharth

PY - 2017

Y1 - 2017

U2 - 10.1016/j.ajhg.2017.08.007

DO - 10.1016/j.ajhg.2017.08.007

M3 - Article

VL - 101

SP - 466

EP - 477

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

SN - 0002-9297

IS - 3

ER -