Results 91 to 100 of about 961 (204)

Apert Syndrome - caveats of squint management. [PDF]

Rom J Ophthalmol, 2023
Khurana R, Singh A, Kochhar D, Sundar S.
europepmc   +1 more source

Apert syndrome and repercussions in Dental Medicine [PDF]

, 2020
Apert’s syndrome is a craniosynostosis syndrome caused by mutations in the gene coding for the fibroblast growthfactor receptor 2 (FGFR2), characterized by craniosynostosis, midface hypoplasia and syndactyly of the hands and feet.
Cardoso, Inês Lopes, Paula, Lígia de
core  

Unraveling the Complexity of Apert Syndrome: Genetics, Clinical Insights, and Future Frontiers. [PDF]

Cureus, 2023
Kumari K, Saleh I, Taslim S, Ahmad S, Hussain I, Munir Z, Javed T, Virk MFI, Javed S, Bisharat P, Ur Rehman U.   +10 more
europepmc   +1 more source

Acrocephalosyndactyly

The American Journal of Medicine, 1972
Max B. Rubin, Donald J. Pirozzi, Charles L. Heaton   +2 more
openaire   +3 more sources

Apert syndrome or type I acrocephalosyndactyly

, 2010
Hani Al Salam
openalex   +1 more source

Seorang Anak Perempuan 1 Bulan Dengan Apert Syndrom (Acrocephalosyndactyly Syndrome Type 1)

, 2022
Tara Nareswari, Farah Hendara Ningrum
openalex   +2 more sources

Apet's Syndrome (Acrocephalosyndactyly. Report of A case) [PDF]

, 1972
Ik Dong Kim, Joo Choul Ihin, Soo Young Lee, Do Soo Park   +3 more
openalex   +1 more source

Apert Syndrome (Acrocephalosyndactyly): A Rare Syndromic Craniosynostosis

, 2009
Mahesh Shrestha, Neelam Adhikari, Ganesh Shah   +2 more
openalex   +2 more sources

Craniosynostosis: Acrocephalosyndactyly (Apert Syndrome) Diagnosed in a Newborn [PDF]

, 2017
Orhideja Stomnaroska, Dragan Danilovski, Sanja Ivanovska   +2 more
openalex   +1 more source

Diagnosing fetal apert syndrome: a case study on prenatal diagnosis and genetic insights. [PDF]

Quant Imaging Med Surg
Ge T, Zhang C, Qi J, Deng X, Du X, Wang Y, Tao J, Zou B, Lin X.   +8 more
europepmc   +1 more source