• A 17q24.3 duplication identified in a large Chinese family with brachydactyly-anonychia
• A case report on autosomal recessive total congenital anonychia
• A novel mutation in the RSPO4 gene in a patient with autosomal recessive anonychia
• A novel nonsense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a Pakistani family
• A patient with total congenital anonychia and depression (author's transl)
• A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22-q11.2
• Acquired anonychia secondary to onychotemnomania
• Acral porokeratosis associated with anonychia
• An infant without nails
• Anonychia
• ANONYCHIA AS A RECESSIVE AUTOSOMAL TRAIT IN MAN
• Anonychia congenita
• Anonychia congenita
• Anonychia Congenita - Rare Inheritance of a Rare Disorder
• Anonychia congenita in different generations of a single Saudi family
• Anonychia congenita totalis: a case report and review of the literature
• Anonychia due to prenatal phenytoin exposure
• Anonychia with absent phalanges and brachydactyly: A report of two unrelated cases
• Anonychia with ectrodactyly: clinical and linkage data
• Brachydactyly-anonychia with congenital absent phalanges of the hand
• Congenital Absence of Nails and Digital-Type Thumb due to Prenatal Phenytoin Exposure
• Congenital anonychia
• Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3
• Congenital anonychia: A distinctive nail finding in a newborn
• Congenital complete anonychia of fingers and toes
• Congenital Nail Disorders among Children with Suspected Ectodermal Dysplasias
• Congenital non-syndromic anonychia totalis with acroosteolysis
• Congenital Non-syndromic Partial Anonychia
• Epidermolysis bullosa and congenital skin aplasia (Bart's syndrome). Report of 3 cases
• Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up
• HYPONYCHIUM ABNORMALITIES Congenital Aberrant Hyponychium vs. Acquired Pterygium Inversum Unguis vs. Acquired Reversible Extended Hyponychium: a proposed classification based on origin, pathology and outcome
• Images in clinical medicine. Epidermolysis bullosa acquisita
• Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I)
• Progressive reticulate skin pigmentation and anonychia in a patient with bone marrow failure
• Pure anonychia
• Rare differentiation disorders: anonychia and ichthyosis of the groin area
• The concept of onychodermis containing onychofibroblasts has histological (microanatomical), immunohistochemical as well as molecular basis
• The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia
• The R-spondin protein family
• Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
• Total anonychia congenita in a woman with normal intelligence: report of a further case
• Total anonychia congenita: a rare heterogeneic disorder
• Total congenital anonychia
• Total congenital anonychia
• Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant