• A case of 12p13.2 heterozygous gene deletion syndrome: congenital thrombocytopenia, ectrodactyly, and tooth deformities
• A Case of Fibular Aplasia-Tibial Campomelia-Oligosyndactyly (FATCO) Syndrome Associated With Split Hand/Foot Syndrome With Long Bone Deficiency (SHFLD) and Review of the Literature
• A case report of Gollop-Wolfgang complex in 12 years old boy
• A complex rearrangement between <em>APC</em> and <em>TP63</em> associated with familial adenomatous polyposis identified by multimodal genomic analysis: a case report
• A complex structural variant near <em>SOX3</em> causes X-linked split-hand/foot malformation
• A Family with EEC Syndrome in the Son and ADULT Syndrome in His Father Caused by the c.797G&gt;A (p.Arg266Gln) Pathogenic Variant in the <em>TP63</em> Gene
• A genotype-phenotype correlation in split-hand/foot malformation type 1: further refinement of the phenotypic subregions within the 7q21.3 locus
• A neonate with Klippel-Trénaunay syndrome: a case report
• A newborn with ectrodactyly, tetralogy of Fallot, esophageal atresia, hypospadias and TP63 gene mutation: A new type of EEC Syndrome?
• A novel de novo TP63 mutation in whole-exome sequencing of a Syrian family with Oral cleft and ectrodactyly
• A Novel Missense Variant of <em>TP63</em> Heterozygously Present in Split-Hand/Foot Malformation
• A rare case of limb deficiency syndrome: Gollop WolfGang syndrome
• A Rare Case Report of Split Hand and Foot Malformation
• A spectrum of TP63-related disorders with eight affected individuals in five unrelated families
• Absent meibomian glands and cone dystrophy in ADULT syndrome: identification by whole exome sequencing of pathogenic variants in two causal genes <em>TP63</em> and <em>CNGB3</em>
• An Unusual Presentation of Bilateral Split Hand-Foot Malformation (SHFM) in Family: A Tale of Two Generations
• Analysis and pharmacological modulation of senescence in human epithelial stem cells
• Atypical presentation of ACCES syndrome resembling dominant Spondyloepiphyseal dysplasia tarda
• BHLHA9 homozygous duplication in a consanguineous family: A challenge for genetic counseling
• Case report: Prenatal diagnosis of Ectrodactyly-Ectodermal dysplasia-Cleft syndrome (EEC) in a fetus with cleft lip and polycystic kidney
• Childbirth and motherhood in women with motor disability due to a rare condition: an exploratory study
• Classifications of split hand foot malformation (SHFM) should include transverse deficiencies: Why Maisels was correct
• Cleft Hand
• Cleft Hand
• Cleft Lip and Palate in Ectodermal Dysplasia
• Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve split-hand/foot malformation type 3
• Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
• Depiction of ectrodactyly, sirenomelia and cyclopia in a figure by Hokusai
• Dermolipoma in a case of split hand/foot malformation: A report of a novel ophthalmic presentation in a rare disease
• Digital Transfer for Hand Reconstruction in Cleft Hand and Foot Differences
• Dynamic correction of ulnar claw hand deformity with a simple insertion into the lumbrical muscle
• Ectodermal dysplasia and cholesteatoma: A cross-sectional analysis of otologic issues
• Ectrodactyly Ectodermal Dysplasia Cleft Lip (EEC) Syndrome
• Ectrodactyly with Polydactyly in a Dog-Case Description and Description of Surgical Therapy with Resection and Fusion Podoplasty
• Ectrodactyly-Ectodermal Dysplasia-Cleft Syndrome: Ocular Findings and Surgical Treatment
• Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome
• Ectrodactyly-ectodermal dysplasia-clefting syndrome. Prenatal prospective ultrasound diagnosis
• Ectrodactyly-lobster claw deformity
• EEC-LM-ADULT syndrome caused by R319H mutation in TP63 with ectrodactyly, syndactyly, and teeth anomaly: A case report
• Expression of DLX6 Gene in Mandibular Deficiency (Retrognathic Mandible): A Randomized Clinical and Genetic Study
• Familial cleft tongue caused by a unique translation initiation codon variant in TP63
• Fatty filum terminale and low-lying conus medullaris in Gollop-Wolfgang complex: a case report and review of literature
• Four Unusual Cases of Congenital Forelimb Malformations in Dogs
• From the Luttrell Psalter to the Lobster Boy: Split hand and foot awaken many facets of human nature
• Functionality Assessment of Patients With Cleft Hands
• Genetic analysis of a Chinese pedigree affected with congenital split-hand/foot malformation
• Genetic predisposition to ocular surface disorders and opportunities for gene-based therapies
• Genome sequencing in families with congenital limb malformations
• Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactyly
• Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in <em>WNT11</em>
• Gollop-Wolfgang Complex: Clinical and Imaging Implications
• Homozygous nonsense mutation of <em>WNT10B</em> gene in a Moroccan family with split-hand foot malformation identified by exome sequencing: a case report
• Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation
• Identification of a Novel TP63 Variant in a Chinese Patient with Orofacial Clefts and Ectrodactyly: Case Report and Literature Review
• Innovative Therapeutic Approaches for the Treatment of the Ocular Morbidities in Patients with EEC Syndrome
• Isoform-Specific Roles of Mutant p63 in Human Diseases
• Lacrimal Drainage Anomalies in Goldenhar, Rubinstein-Taybi, and Ectodermal-Ectrodactyly-Clefting Syndromes
• Maxillomandibular Fusion Along with Fusion of Dorsal Surface of the Tongue to the Hard Palate-A Case Report
• Medical findings and congenital anomalies in Vermeer's paintings
• Microduplication of BTRC detected in a Chinese family with split hand/foot malformation type 3
• Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling
• Mosaicism in Hartsfield syndrome
• New pathogenic variant in <em>DLX5</em>: New clues for a clinical spectrum from split-hand-foot malformation to fibular aplasia, tibial campomelia and oligosyndactyly
• Newborn Male With Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome: A New Case Report Putting the Condition Under Spotlight
• Novel HOXD13 variants in syndactyly type 1b and type 1c, and a new spectrum of TP63-related disorders
• Ocular Manifestations in Patients Affected by p63-Associated Disorders: Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) and Ankyloblepharon-Ectodermal Defects-Cleft Lip Palate (AEC) Syndromes
• Ocular manifestations of ectodermal dysplasia
• Ocular Manifestations of Ectrodactyly-Ectodermal Dysplasia-Cleft Palate (EEC) Syndrome: A Case Report
• Oral management of children/adolescents with ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome: A scoping review
• Osteogenesis Imperfecta and Split Foot Malformation due to 7q21.2q21.3 Deletion Including COL1A2, DLX5/6 Genes: Review of the Literature
• Overlap between EEC and AEC syndrome and immunodeficiency in a preterm infant with a TP63 variant
• p63 in corneal and epidermal differentiation
• Peripheral giant cell granuloma in a child with ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome: a case report
• PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation
• Pre-natal and post-natal diagnosis of congenital upper limb differences: The first 3 years of the Australian Hand Difference Register
• Prenatal diagnosis of Hartsfield syndrome with a novel genetic variant
• Prevalence rates for ectodermal dysplasia syndromes
• Prosthetic rehabilitation of a patient with ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome through a hybrid workflow: A case report with 2-year follow-up
• Rare association of trisomy 13 with ectrodactyly and congenital diaphragmatic hernia
• Sequence Variants in the <em>WNT10B</em> and <em>TP63</em> Genes Underlying Isolated Split-Hand/Split-Foot Malformation
• Sequence Variants in the <em>WNT10B</em> Underlying Non-Syndromic Split-Hand/Foot Malformation
• SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably
• Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report
• Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the <em>DLX5/6</em> Genes
• Split-hand/foot malformation 3 resulting from microduplications in 10q24 region in five patients from India
• Structural and functional foot disorders in patients with genodermatoses: a single-centre, retrospective chart review
• Structural model of human PORCN illuminates disease-associated variants and drug-binding sites
• Surgical Treatment of Ulnar Cleft Hand with All Fingers - A Report of Two Patients
• The first reported case of <em>CDH3</em>-related hypotrichosis with juvenile macular dystrophy from Jordan: a case report
• The molecular genetics of human appendicular skeleton
• The power of zebrafish models for understanding the co-occurrence of craniofacial and limb disorders
• The prenatal diagnosis and genetic counseling of chromosomal micro-duplication on 10q24.3 in a fetus: A case report and a brief review of the literature
• TP63-mutation as a cause of prenatal lethal multicystic dysplastic kidneys
• TP63-related disorders: two case reports and a brief review of the literature
• Treatment and Management of Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome With Scleral Prosthetic Devices
• Treatment of Cleft Foot Deformity using Fish Mouth Incision and Suture-Button in Paediatric Foot: A case report
• UBA2 variants underlie a recognizable syndrome with variable aplasia cutis congenita and ectrodactyly
• Ulnocarpal arthrodesis as a new treatment for ectrodactyly in a dog and a cat
• Variable clinical presentation of split hand/foot malformation syndrome in a family with microduplication of 10q24.32: a case report
• Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family