• A case of severe proximal focal femoral deficiency with overlapping phenotypes of Al-Awadi-Raas-Rothschild syndrome and Fuhrmann syndrome
• A morpho-etiological description of congenital limb anomalies
• A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
• A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus
• A report of two cases of Al-Awadi Raas-Rothschild syndrome (AARRS) supporting that "apparent" Phocomelia differentiates AARRS from Schinzel Phocomelia syndrome (SPS)
• ADIPOQ gene polymorphisms and haplotypes linked to altered susceptibility to PCOS: a case-control study
• Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation
• Al-Awadi/Raas-Rothschild syndrome in a newborn with additional anomalies
• Clustering of trisomy 18 in Kuwait: Genetic predisposition or environmental?
• Congenital para esophageal hernia: a 10 year experience from Saudi Arabia
• Connexin 26 gene mutations in non-syndromic hearing loss among Kuwaiti patients
• High survival rate in childhood non-Hodgkin lymphoma without CNS involvement: results of BFM 95 study in Kuwait
• Identification of novel differentially expressed genes in type 1 diabetes mellitus complications using transcriptomic profiling of UAE patients: a multicenter study
• Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing
• Molecular basis of the clinical features of Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome (AARRS) and Fuhrmann syndrome
• Nationwide study of rates of reinfection with SARS-CoV-2 among adults in Kuwait
• Profile of major congenital malformations in neonates in Al-Jahra region of Kuwait
• Relation of resistin gene variants to resistin plasma levels and altered susceptibility to polycystic ovary syndrome: A case control study
• The high-molecular weight multimer form of adiponectin is a useful marker of polycystic ovary syndrome in Bahraini Arab women
• The WNT7A G204S mutation is associated with both Al-Awadi-Raas Rothschild syndrome and Fuhrmann syndrome phenotypes
• Toxoplasma gondii Infection Among Institutionalized Children with Down syndrome in Sana'a city, Yemen: Implications of Low IgG Seroprevalence
• Transthyretin Gene Mutation Associated with Familial Carpal Tunnel Syndrome in Sample of Iraqi Patients
• Unilateral ovarian diathermy prior to successful in vitro fertilisation: a strategy to prevent recurrence of ovarian hyperstimulation syndrome?