Results 101 to 110 of about 790 (167)

Acrocephalosyndactyly Syndrome: Challenging Diagnosis

Journal of Case Reports, 2017
Ada Paloma Soto Brambila, Paloma Rivero Moragrega, Ingrid Patricia Dávalos Rodríguez, Juan Francisco Santoscoy Gutiérrez   +3 more
openaire   +2 more sources

Malformation Pattern and Molecular Findings in the FGFR1-Related Hartsfield Syndrome Phenotype. [PDF]

Med Sci (Basel)
Gaudioso F, Pascolini G.
europepmc   +1 more source

Contemporary Management of the Upper Limb in Apert Syndrome: A Review. [PDF]

Plast Reconstr Surg Glob Open
Khabyeh-Hasbani N, Lu YH, Baumgartner W, Mendenhall SD, Koehler SM.   +4 more
europepmc   +1 more source

Hearing Loss and Chiari Malformation Type I: A Scoping Review. [PDF]

Diseases
Migliorelli A, Manuelli M, Bianchini C, Stomeo F, Pelucchi S, Palma S, Ciorba A.   +6 more
europepmc   +1 more source

Ruptured intracranial dermoid cyst with progressive spinal dissemination: illustrative case. [PDF]

J Neurosurg Case Lessons
Paul U, Owusu-Adjei B, Mietus CJ, Karandikar P, Cataltepe O.   +4 more
europepmc   +1 more source

Stuck Together: A Systematic Review of Hand Syndactyly. [PDF]

Cureus
Gowrie S, Omosebi O, Veith P, Agarwal N, Shah S, Montalbano M, Tubbs RS, Loukas M.   +7 more
europepmc   +1 more source

Molecular Regulation of Craniofacial Bone and Palate Development [PDF]

, 2004
Rice, Ritva
core  

TWIST1 Gene Variants Cause Craniosynostosis with Limb Abnormalities in Asian Patients. [PDF]

J Pediatr Genet
Dhiman S, Panigrahi I, Sharma M, Chaudhry C, Garg M.   +4 more
europepmc   +1 more source

Benefit/risk balance of prone positioning as first line treatment for upper airway obstruction in Robin sequence. [PDF]

Eur J Pediatr
Adnot P, Vegas N, Coutier L, Gras Leguen C, Giuseppi A, Aubineau Y, Khirani S, Soupre V, Luscan R, Fauroux B, Abadie V.   +10 more
europepmc   +1 more source