Malformation Pattern and Molecular Findings in the <i>FGFR1</i>-Related Hartsfield Syndrome Phenotype. [PDF]
Gaudioso F, Pascolini G.
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A Case of Pfeiffer Syndrome Type 1
Ali Karaman, Fuat Laloğlu, Remzi Arslan
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CPT Codes for Pediatric Orthopaedics. [PDF]
Dale Blasier R, Neal K.
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KCNQ1 and GJA1 Variants Associated With Arrhythmogenic Right Ventricular Cardiomyopathy With a Lethal Outcome. [PDF]
Tramèr L +9 more
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CONGENITAL ANOMALIES OF THE UPPER LIMBS IN A UNIVERSITY CENTER: A CROSS-SECTIONAL STUDY. [PDF]
Gomes DJL +5 more
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Frem2 knockout mice exhibit Fraser syndrome phenotypes and neonatal lethality due to bilateral renal agenesis. [PDF]
Simikyan RG +9 more
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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]
Alzein HH +4 more
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Isolated Unilateral Heptadactyly With Combined Preaxial and Postaxial Polydactyly of the Foot in a 9-Month-Old Infant. [PDF]
Mallilah BP +4 more
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Clinical and biological impact of caffeine therapy in premature infants with apnea of prematurity: a prospective observational study. [PDF]
Neamțu AV +11 more
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Fraser Syndrome: A Narrative Review Based on a Case from Vietnam and the Past 20 Years of Research. [PDF]
Thi Pham XT, Nguyen PN, Hoang XS.
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