• Analysis of two candidate genes for Basan syndrome
• Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma
• Basan gets a new fingerprint: Mutations in the skin-specific isoform of SMARCAD1 cause ectodermal dysplasia syndromes with adermatoglyphia
• BASAN index (Body mass index, Age, Sex, Arterial hypertension and Neck circumference) predicts severe apnoea in adults living at high altitude
• Basan syndrome in a family from South India: a novel SMARCAD1 variant
• Basan syndrome in family from South-India: A novel SMARCAD1 variant
• Basan's syndrome: Congenital absence of dermatoglyphs and milia
• Basan's syndrome: dominant autosomal hypohidrotic ectodermal dysplasia
• Ectodermal dysplasia with congenital adermatoglyphia (Basan syndrome): Report of two cases presenting with extensive congenital milia
• Effects of alcohol withdrawal on blood pressure in hypertensive heavy drinkers
• Evaluation of Urinalysis-Based Screening for Urothelial Carcinoma in Patients With Lynch Syndrome
• Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome
• Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964)
• Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndrome
• Plasma adiponectin is decreased in nonalcoholic fatty liver disease
• Profuse congenital familial milia with absent dermatoglyphics (Basan's Syndrome): description of a new family
• Retracted: Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma
• Two <em>SMARCAD1</em> Variants Causing Basan Syndrome in a Canadian and a Dutch Family
• Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family