• "Bibloc advancement" with a combination of internal and external distracters
• 1.7 cm elongated Achilles tendon did not alter walking gait kinematics 4.5 years after non-surgical treatment
• A cross-sectional study of long-term satisfaction after surgery for congenital syndactyly: does skin grafting influence satisfaction?
• A Cross-Sectional Study of the Neuropsychiatric Phenotype of CACNA1C-Related Disorder
• A FURTHER PATIENT OF PURE 15q DELETION: CLINICAL AND MOLECULAR CYTOGENETIC FINDINGS
• A human embryonic limb cell atlas resolved in space and time
• A new surgical procedure for little toe polysyndactyly without skin graft
• A podoscopic and descriptive study of foot deformities in patients with Down syndrome
• A Ser252Trp substitution in mouse FGFR2 results in hyperplasia of embryonic salivary gland parenchyma
• A toe keloid after syndactyly release treated with surgical excision and intralesional steroid injection
• Abnormalities of developmental cell death in Dad1-deficient mice
• Absence of post-translational aspartyl beta-hydroxylation of epidermal growth factor domains in mice leads to developmental defects and an increased incidence of intestinal neoplasia
• Advancement Flaps
• An Additional Lrp4 High Bone Mass Mutation Mitigates the Sost-Knockout Phenotype in Mice by Increasing Bone Remodeling
• An anatomical classification of congenital proximal radioulnar synostosis based on retrospective MRI measurement combined with radiography
• Anatomical Differences Between Foot and Hand Web Space Reconstruction
• Apert syndrome mutant FGFR2 and its soluble form reciprocally alter osteogenesis of primary calvarial osteoblasts
• Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A
• Associations between different heart rate variability ratios and cardiometabolic risk factors in young adults
• Autonomic and cardiorespiratory responses to the active tilt test in individuals with Parkinson disease: cross-sectional study
• Avoidance of a potential tracheoinnominate fistula by innominate artery re-implantation in a four year old girl with tracheostomy dependence and Pfeiffer syndrome
• Awareness about Patterson syndrome among dental students
• BMPs are direct triggers of interdigital programmed cell death
• Carrier frequency and incidence estimation of Smith-Lemli-Opitz syndrome in East Asian populations by Genome Aggregation Database (gnomAD) based analysis
• Case report: Syndactyly in German Holstein calves
• Cenani-Lenz syndactyly in a patient with features of Kabuki syndrome
• Cenani-Lenz syndrome and other related syndactyly disorders due to variants in LRP4, GREM1/FMN1, and APC: Insight into the pathogenesis and the relationship to polyposis through the WNT and BMP antagonistic pathways
• Cerebral and cerebellar white matter abnormalities with magnetic resonance imaging in a child with Feingold syndrome
• Children with Apert syndrome as adults: a follow-up study of 28 Scandinavian patients
• Complex postaxial polydactyly types A and B with camptodactyly, hypoplastic third toe, zygodactyly and other digit anomalies caused by a novel GLI3 mutation
• Congenital hand differences: Prevalence among school going children in Mangalore city
• Congenital Maxillomandibular Synechia with Multiple Malformations in a Very-Low-Birth-Weight Infant: A Case Report
• Congenital syndactyly in cattle: four novel mutations in the low density lipoprotein receptor-related protein 4 gene (LRP4)
• Cooperation of BMP and IHH signaling in interdigital cell fate determination
• Correlation among Poincare plot and traditional heart rate variability indices in adults with different risk levels of metabolic syndrome: a cross-sectional approach from Southern India
• Cross-cultural translation, reliability and validity of the Thai version of the Patient-Reported Outcomes Measurement Information System (PROMIS) Parent Proxy Upper Extremity Short Form 8a in children with congenital upper extremity anomalies
• Cross-cultural translation, reliability and validity of the Thai version of the Patient‑Reported Outcomes Measurement Information System (PROMIS) Parent Proxy Upper Extremity Short Form 8a in children with congenital upper extremity anomalies
• Crossed polydactyly and Greig cephalopolysyndactyly syndrome
• Dancing girl flap: a new flap suitable for web release
• Deformed Skull Morphology Is Caused by the Combined Effects of the Maldevelopment of Calvarias, Cranial Base and Brain in FGFR2-P253R Mice Mimicking Human Apert Syndrome
• Descriptive epidemiology of hereditary musculoskeletal and limb defects in the isolated population of Chitral, North-West Pakistan
• Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy
• Dorso Proximal Interphalangeal Island Flap
• Evaluation of cardiac autonomic function and low-grade inflammation in children with obesity living in the Northeast Brazilian region
• Familial crossed polysyndactyly in four generations of an Indian family
• Filippi syndrome: report of three additional cases
• fras1 shapes endodermal pouch 1 and stabilizes zebrafish pharyngeal skeletal development
• From Mendel laws to whole genetic association study to decipher the swine mulefoot phenotype
• Gene mutations and genomic rearrangements in the mouse as a result of transposon mobilization from chromosomal concatemers
• Genetic Subtypes of Apert Syndrome Are Associated With Differences in Airway Morphology and Early Upper Airway Obstruction
• Genetics analysis of mouse mutations Abnormal feet and tail and rough coat, which cause developmental abnormalities and alopecia
• Heart Rate Variability Analysis May Identify Individuals With Williams-Beuren Syndrome at Risk of Sudden Death
• Heavy metals and trace elements in maternal blood and prevalence of congenital limb abnormalities among newborns: the Japan Environment and Children's Study
• Hemimelic extra toes and Hammer toe are distinct mutations that show a genetic interaction
• Hereditary syndactyly in Angus cattle
• Hot cross bun sign and prominent cerebellar peduncle involvement in a patient with oculodentodigital dysplasia
• Inducible and reversible regulation of endogenous gene in mouse
• Infant with a big head and 'crossed' polysyndactyly
• Infant with a big head and 'crossed' polysyndactyly
• Intellectual, behavioral, and emotional functioning in children with syndromic craniosynostosis
• Interconnection between Mixed-Handedness, Digit Ratios and Hand and Foot Minor Anomalies in Predicting Schizophrenia
• Long-Term Outcome of Digital Defect Reconstruction using Cross-Finger Flaps
• Maxillary Changes Following Facial Bipartition - A Three-Dimensional Quantification
• Measuring parent proxy-reported quality of life of 11 rare diseases in children in Zhejiang, China
• Megalencephaly syndromes: exome pipeline strategies for detecting low-level mosaic mutations
• Modification of the effects of nitrogen dioxide and sulfur dioxide on congenital limb defects by meteorological conditions
• Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesis
• Nasopharyngeal airway and subcranial space analysis in Pfeiffer syndrome
• Normative data for anthropometric parameters used in delineation of dysmorphic features in north Indian children
• NOVEL <em>XRCC4</em> MUTATIONS IN AN INFANT WITH MICROCEPHALIC PRIMORDIAL DWARFISM, DILATED CARDIOMYOPATHY, SUBCLINICAL HYPOTHYROIDISM, AND EARLY DEATH: EXPANDING THE PHENOTYPE OF <em>XRCC4</em> MUTATIONS
• Oculodentodigital Dysplasia with a Novel Mutation in <em>GJA1</em> Diagnosed by Targeted Gene Panel Sequencing: A Case Report and Literature Review
• Ophthalmic findings in apert syndrome prior to craniofacial surgery
• Oral health status of children with syndromic craniosynostosis
• Patients with sclerosteosis and disease carriers: human models of the effect of sclerostin on bone turnover
• Pattern of congenital hand anomalies at a tertiary plastic surgery service in South-Western Nigeria: A 10-year, cross-sectional retrospective review
• Patterns of tooth agenesis in patients with crouzon or apert syndrome
• Peripartum hysterectomy clinical characteristics and outcomes- a hospital based retrospective audit study
• Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations
• Poland syndrome
• Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndrome
• Prevalence of Hand Malformations in Patients With Moebius Syndrome and Their Management
• Production of a mouse line with a conditional Crim1 mutant allele
• Relationship between the number of comorbidities, quality of life, and cardiac autonomic modulation in patients with coronary disease: a cross-sectional study
• Relationships among manual body functions, manual capacity, and bimanual performance using the prosthetic upper extremity functional index in children with congenital hand differences
• Renal phenotype is exacerbated in Os and lpr double mutant mice
• Respiratory pattern complexity in newly-diagnosed asthmatic patients
• Retroauricular full-thickness skin grafts in syndactyly repair: outcome and comparison with inguinal full-thickness skin grafts: retrospective (cross-sectional) study
• Serum Dickkopf 1 levels in sclerostin deficiency
• Stable Recombinant Invasion Plasmid Antigen C (IpaC)-Based Single Dose Nanovaccine for Shigellosis
• The assessment of midface distraction osteogenesis in treatment of upper airway obstruction
• The bovine aristaless-like homeobox 4 (ALX4) as a candidate gene for syndactyly
• The Classification of Swanson for Congenital Anomalies of Upper Limb Modified by the Japanese Society for Surgery of the Hand (JSSH)
• The cross incision plasty for reconstruction of the burned web space: introduction of an alternative technique for the correction of dorsal and volar neosyndactyly
• The incidence of cleft lip and palate in Addis Ababa, Ethiopia
• The Modified 3-square Flap Method for Reconstruction of Toe Syndactyly
• The mutation spectrum in Holt-Oram syndrome
• Three-dimensional analysis of the palatal morphology in growing patients with Apert syndrome and Crouzon syndrome
• Uncombable hair (cheveux incoiffables, pili trianguli et canaliculi) syndrome: brief review and role of scanning electron microscopy in diagnosis
• Unique case of polydactyly and a new classification system
• Usefulness of a palmar crease template for the treatment of complicated syndactyly