Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause Klippel-Feil Anomaly

publication

Journal Article

2013

Published in:

Alkuraya, Jawahir Y. Mohamed, Eissa Faqeih, Abdulmonem Alsiddiky, Muneera J. Alshammari, Niema A. Ibrahim, and Fowzan S. . 2013

قراءة

Publication Work Type

دكتوراة

Volume Number

Issue Number

Magazine \ Newspaper

The American Journal of Human genetics

Pages

175-161

more of publication

EFFICACY OF SINGLE STAGE MULTILEVEL SOFT TISSUE RELEASE BY PERCUTANEOUS NEEDLE TECHNIQUE FOR SPASTIC CONTRACTURES OF LOWER LIMBS IN CEREBRAL PALSY

by Abdulmonem M. Alsiddiky, SSC-Orth*, Khalid A. Bakarman, ABOS, Kholoud O. Alzain, SSC-Orth, Zulqurnain Rafiq, FCP, Ibrahim Alshaygy, SSC-Orth, Fahad Alhuzaimi, SSC-Orth, Waleed Awwad, FRCSC, Abdel Rahman M. Zamzam, MSc and Muhammed Asif

2017

Humeral lateral condyle fractures in children: redefining the criteria for displacement

by Khalid A. Bakarman, Abdul Monem M. Alsiddiky, Kholoud O. Alzain, Hazem M. Alkhawashki, Ahmed S. Bin Nasser, Khalid A. Alsaleh, Fawzi F. Al-Jassir and Mohamed M. Zamzam

2016

Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue

by Anas M. Alazami · Sarah M. Al‑Qattan · Eissa Faqeih · Amal Alhashem · Muneera Alshammari1 · Fatema Alzahrani1 · Mohammed S. Al‑Dosari1 · Nisha Patel · Afaf Alsagheir · Bassam Binabbas · Hamad Alzaidan · Abdulmonem Alsiddiky · Nasser Alharb

2016

عبدالمنعم بن محمد الصديقي

Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause Klippel-Feil Anomaly

Alkuraya, Jawahir Y. Mohamed, Eissa Faqeih, Abdulmonem Alsiddiky, Muneera J. Alshammari, Niema A. Ibrahim, and Fowzan S. . 2013