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1. 母斑性基底細胞癌症候群 nevoid basal cell carcinoma syndrome
2. 遺伝性皮膚症 the genodermatoses
3. 基底細胞癌の疫学および臨床的特徴 epidemiology and clinical features of basal cell carcinoma
4. 髄芽腫の組織病理および分子学的病因 histopathology and molecular pathogenesis of medulloblastoma
5. 脳腫瘍の危険因子 risk factors for brain tumors

Airway management of a child with frontometaphyseal dysplasia (Gorlin Cohen syndrome).

Ganigara A, Nishtala M, Chandrika YR, Chandrakala KR.
Journal of anaesthesiology, clinical pharmacology.J Anaesthesiol Clin Pharmacol.2014 Apr;30(2):279-80. doi: 10.4103/0970-9185.130100.
Frontometaphyseal dysplasia (FMD), also called Gorlin-Cohen syndrome, is a rare hereditary X-linked dominant craniotubular bone disorder. The presentation describes the airway management of a 2-year-old child suffering from FMD with significant retrognathia, posted for major long bone corrective ost
PMID 24803775

Treatment of obstructive uropathy in one of three young brothers suffering from Gorlin-Cohen syndrome: a case report.

Vakalopoulos I1, Kampantais S, Dimopoulos P, Papastavros C, Katsikas V.
BMC urology.BMC Urol.2012 Jan 10;12:2. doi: 10.1186/1471-2490-12-2.
BACKGROUND: Frontometaphyseal dysplasia, or Gorlin-Cohen syndrome, is an X-linked disorder primarily characterized by skeletal dysplasia, such as hyperostosis of the skull and abnormalities of tubular bone modeling. Some patients develop extraskeletal manifestations, such as urinary tract anomalies.
PMID 22233653

Foot deformity in frontometaphyseal dysplasia (Gorlin-Cohen syndrome): a case report.

Vinay S1, Andreas R, Bernhard ZE, Gerhardt S.
The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons.J Foot Ankle Surg.2000 Mar-Apr;39(2):131-5.
A case of frontometaphyseal dysplasia (Gorlin-Cohen syndrome) in a child is described. The boy showed characteristic musculoskeletal changes, and had bilateral symptomatic cavovarus deformities of the feet. Surgical management of the foot deformities and the outcome are discussed.
PMID 10789105