Malformation Pattern and Molecular Findings in the FGFR1-Related Hartsfield Syndrome Phenotype. [PDF]
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Fraser Syndrome: A Report of Two Cases
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Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies [PDF]
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A Systematic Review of Digital Deformities in Pediatric Patients and Their Podiatric Treatments. [PDF]
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CONGENITAL ANOMALIES OF THE UPPER LIMBS IN A UNIVERSITY CENTER: A CROSS-SECTIONAL STUDY. [PDF]
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KCNQ1 and GJA1 Variants Associated With Arrhythmogenic Right Ventricular Cardiomyopathy With a Lethal Outcome. [PDF]
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Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly [PDF]
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Surgical Correction of a Severe Bilateral Cleft Foot Using a Diamond Incision and Cannulated Screw Fixation: A Case Report and Literature Review. [PDF]
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Maternal exposure to ambient air pollution and risk of congenital limb defects in offspring. [PDF]
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Experience with patients presenting with the clinical features of Holt-Oram syndrome: a single center retrospective study. [PDF]
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