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Clinical Case Reports|July 18, 2015
Nine de novo duplications affecting both maternal and paternal chromosomes and an inherited 15q11.2 deletion, in a patient with developmental delayMarwan K Tayeh, Tracy Rocco, Todd Ackley, et al.Saudi Medical Journal|November 19, 2002
Linkage analysis of a large inbred family with congenital megaloblastic anemiaJamil R Al-Alami, Marwan K Tayeh, Mahmoud Y Al-Sheyyab, et al.Saudi Medical Journal|July 28, 2005
Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 in JordanJamil R Al-Alami, Stephan M Tanner, Marwan K Tayeh, et al.Human Molecular Genetics|January 10, 2006
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionHsan-Jan Yen, Marwan K Tayeh, Robert F Mullins, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 14, 2009
Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplicationsMarwan K Tayeh, Ephrem L H Chin, Vanessa R Miller, et al.American Journal of Medical Genetics. Part A|April 2, 2022
Novel multilocus imprinting disturbances in a child with expressive language delay and intellectual disabilityMarwan K Tayeh, Janean DeVaul, Kristin LeSueur, et al.Human Molecular Genetics|April 3, 2008
Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterningMarwan K Tayeh, Hsan-Jan Yen, John S Beck, et al.Saudi Medical Journal|October 28, 2003
Familial Mediterranean fever mutation frequencies and carrier rates among a mixed Arabic populationJamil R Al-Alami, Marwan K Tayeh, Dana A Najib, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 18, 2022
Clinical pharmacogenomic testing and reporting: A technical standard of the American College of Medical Genetics and Genomics (ACMG)Marwan K Tayeh, Andrea Gaedigk, Matthew P Goetz, et al.Clinical Diabetes and Endocrinology|April 4, 2018
Potential association of LMNA-associated generalized lipodystrophy with juvenile dermatomyositisMelis Sahinoz, Shafaq Khairi, Ashley Cuttitta, et al.Pageof 2