B. Meyer

A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy

M. Zou, Yufei Shi, A. Shati, 2015, International journal of endocrinology.

Novel homozygous mutation in DSP causing skin fragility–woolly hair syndrome: report of a large family and review of the desmoplakin‐related phenotypes

O. Khalifa, H. Al-Hindi, S. Wakil, 2011, Clinical genetics.

A novel syndrome of abnormal striatum and congenital cataract: evidence for linkage to chromosomes 11

N. Kaya, D. Çolak, A. Al-Bakheet, 2013, Clinical genetics.

A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia

G. Morahan, N. Dzimiri, B. Meyer, 2017, Clinical genetics.

A common variant association study reveals novel susceptibility loci for low HDL‐cholesterol levels in ethnic Arabs

G. Morahan, N. Dzimiri, B. Meyer, 2016, Clinical genetics.

Smith–Lemli–Opitz syndrome among Arabs

J. Al-Aama, E. Faqeih, Z. Al-Hassnan, 2012, Clinical genetics.

Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia

S. Bohlega, S. Wakil, B. Meyer, 2014, Clinical genetics.