Results 81 to 90 of about 790 (167)

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

DOMINANT ACROCEPHALOSYNDACTYLY [PDF]

Hereditas, 2010
openaire   +1 more source

Prenatal diagnosis of craniosynostosis: a case description and genetic evaluation. [PDF]

Quant Imaging Med Surg
Tang ZF, Lin XJ, Deng L, Yang T, Yang L.
europepmc   +1 more source

Silent Chiari Type I Malformation Presenting With Markedly Asymmetrical Papilledema Detected on Routine Ophthalmic Examination: A Pediatric Case Report. [PDF]

Cureus
Cömerter D, Öz FR, Ayaz Kaya D.
europepmc   +1 more source

Introductory Chapter: Acne and Acneiform Dermatoses [PDF]

, 2017
Gönül, Müzeyyen, Kartal, Selda Pelin
core   +1 more source

Type I Acrocephalosyndactyly [PDF]

, 2020
openaire   +1 more source

Concurrent surgical management of pineoblastoma and Chiari type 1.5 malformation: a case report. [PDF]

BMC Surg
Yiğit H, Gökoğlu A.
europepmc   +1 more source

Apert Syndrome: An Insight Into Dentofacial Features. [PDF]

Cureus, 2021
Jose B, Emmatty TB, Methippara JJ, Kumar K, Thampi NM.   +4 more
europepmc   +1 more source

From FGFR2 mutations to precision management: a review of prenatal diagnosis and multidisciplinary interventions in apert syndrome. [PDF]

Front Pediatr
Li H, Shen J, Tang M, Wan S, Zhang S.
europepmc   +1 more source

A novel FGFR2 (S137W) mutation resulting in Apert syndrome: A case report. [PDF]

Medicine (Baltimore), 2020
Shi Q, Dai R, Wang R, Jing J, Yu X, Liu R, Liu Y.   +6 more
europepmc   +1 more source