• A case report of prenatally diagnosed ophthalmo-acromelic syndrome type Waardenburg
• A fetal case of microphthalmia and limb anomalies with abnormal neuronal migration associated with SMOC1 biallelic variants
• A locus for ophthalmo-acromelic syndrome mapped to 10p11.23
• A novel homozygous variant in the SMOC1 gene underlying Waardenburg anophthalmia syndrome
• A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome
• Anophthalmia-Waardenburg syndrome or ophthalmo-acromelic syndrome: what is in a name?
• Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and review
• Artificial intelligence and machine learning tools for high-performance microalgal wastewater treatment and algal biorefinery: A critical review
• Bilateral microphthalmia with cyst, facial clefts, and limb anomalies: a new syndrome with features of Waardenburg syndrome, cerebro-oculo-nasal syndrome, and craniotelencephalic dysplasia
• Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice
• Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice
• Mutations in the SPARC-related modular calcium-binding protein 1 gene, SMOC1, cause waardenburg anophthalmia syndrome
• Ophthalmo acromelic syndrome
• Ophthalmo-acromelic syndrome
• Ophthalmo-acromelic syndrome (Waardenburg) with split hand and polydactyly
• Ophthalmo-acromelic syndrome in a Turkish infant: case report
• Ophthalmo-acromelic syndrome in an infant
• Ophthalmo-acromelic syndrome: report and review
• Ophthalmo-acromelic syndrome: report of a case with vertebral anomalies
• PORCN-related microphthalmia with limb anomalies: Case report and literature review
• Progressive scoliosis associated with microphthalmia with limb anomalies: A case report
• Secreted modular calcium-binding proteins in pathophysiological processes and embryonic development
• SMOC1 is essential for ocular and limb development in humans and mice
• Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies