C. Tan

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

K. Friend, M. Shaw, E. Haan, 2015, Molecular Psychiatry.

H2AX gene does not have a modifier effect on ataxia‐telangiectasia phenotype

L. Mesci, Ö. Sanal, C. Tan, 2011, International journal of immunogenetics.

Genotype/phenotype correlations in X-linked dominant Charcot-Marie-Tooth disease.

W. Brown, C. Bolton, P. Ainsworth, 1999, Annals of the New York Academy of Sciences.

Skewing of X‐chromosome inactivation in three generations of carriers with X‐linked chronic granulomatous disease within one family

O. Sanal, I. Tezcan, M. de Boer, 2006, European journal of clinical investigation.

Characteristics of patients with C1 esterase inhibitor deficiency: a single center study.

C. Tan, D. Çağdaş, E. Aytekin, 2020, European annals of allergy and clinical immunology.

Analysis of ASPM in an ethnically diverse cohort of 400 patient samples: perspectives of the molecular diagnostic laboratory

D. del Gaudio, K. Arndt, S. Das, 2014, Clinical genetics.