نتائج البحث

Molecular analysis of exons 8, 9 and 10 of the fibroblast growth factor receptor 2 (FGFR2) gene in two families with index cases of apert syndrome ; Análisis molecular de los exones 8, 9 y 10 del gen del factor de crecimiento de fibroblastos (FGFR2) en dos familias con casos índice de síndrome de apert

• Authors : Torres L.; Hernández G.; Barrera A.

Subjects: Fibroblast growth factor receptor 2; Acrocephalosyndactyly; Article

• Source: instname:Universidad del Rosario

تفاصيل العنوان

Apert syndrome: Diagnostic and management problems in a resource-limited country

• Authors : Boubacar Nacro; Fatimata Sahoura Nacro; Alain Saga Ouermi

Subjects: medicine.medical_specialty; Pediatrics; lcsh:Medicine

• Source: Pediatric Reports, Vol 11, Iss 4 (2019)Pediatric ReportsVolume 11Issue 4

تفاصيل العنوان

Apert syndrome

• Authors : Kılıç, Ä°lknur.; Baykara, Y.; Semerci, Cavidan Nur.

Subjects: Apert syndrome; FGFR2 mutation; fibroblast growth factor receptor 2

تفاصيل العنوان

Discussão genético-clínica sobre a sindrome de Apert a propósito de um caso

• Authors : Goncalves, A.; Silva, J. B. da; Universidade Estadual Paulista (UNESP)

Subjects: acrocephalosyndactyly; diagnosis; major clinical study

تفاصيل العنوان

Anesthetic management of craniosynostosis repair in patient with Apert syndrome

• Authors : Niraj Kumar; Keshav Goyal; Ashish Bindra

Subjects: medicine.medical_specialty; Heart disease; business.industry

• Source: Saudi Journal of Anaesthesia, Vol 8, Iss 3, Pp 399-401 (2014)Saudi Journal of Anaesthesia

تفاصيل العنوان

Discussão genético-clínica sobre a sindrome de Apert a propósito de um caso

• Authors : Goncalves, A.; Silva, J. B. da; Universidade Estadual Paulista (UNESP)

Subjects: acrocephalosyndactyly; diagnosis; major clinical study

تفاصيل العنوان

Tripod-shaped Syndactyly in Apert Syndrome with FGFR2 p.P253R Mutation

• Authors : Biswajit Mishra; Rashmi Patel; Chandrabhan Singh

Subjects: musculoskeletal diseases; congenital, hereditary, and neonatal diseases and abnormalities; RD1-811

• Source: Indian Journal of Plastic Surgery, Vol 54, Iss 03, Pp 370-372 (2021)Indian Journal of Plastic Surgery : Official Publication of the Association of Plastic Surgeons of India

تفاصيل العنوان

A Case of Saethre-Chotzen Syndrome

• Authors : McKeon-Kern, Catherine; Mamunes, Peter

Subjects: Human Genetics; Case Report; Saethre-Chotzen

• Source: MCV/Q, Medical College of Virginia Quarterly

تفاصيل العنوان