L.I. Al-Gazali

Mutations in the Transmembrane Natriuretic Peptide Receptor NPR-B Impair Skeletal Growth and Cause Acromesomelic Dysplasia, Type Maroteaux

Cynthia F. Bartels, Hülya Bükülmez, Pius S. Padayatti et al. · The American Journal of Human Genetics · 2004 · 363 citations · Full text

Sclerostin, Signal Transduction, Molecular Physiology +8

Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development

Michael A. Simpson, Ray C. J. Hsu, Lindsay Keir et al. · The American Journal of Human Genetics · 2007 · 225 citations · Full text

Bone Disease, Genetic Disorder, Genetics +9

Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome

Nathalie Dagoneau, Déborah Scheffer, Céline Huber et al. · The American Journal of Human Genetics · 2004 · 183 citations · Full text

Genetic Disorder, Genetics, Pathology +4

The profile of major congenital abnormalities in the United Arab Emirates (UAE) population.

L.I. Al-Gazali, Adekunle Dawodu, K Sabarinathan et al. · Journal of Medical Genetics · 1995 · 124 citations · Full text

Down Syndrome, Developmental Anomaly, Major Malformations +15

Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?

Tamás Révész, Sophie Fletcher, L.I. Al-Gazali et al. · Journal of Medical Genetics · 1992 · 118 citations · Full text