Oculocerebrocutaneous syndrome.

Author:

Bleeker-Wagemakers L M,Hamel B C,Hennekam R C,Beemer F A,Oorthuys H W

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference16 articles.

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2. Reference Prenatal exclusion testing for Huntington's disease: a problem of too much information;Millan, F.A.; Curtis, A.; Mennie, M.;Med Genet,1989

3. Prenatal exclusion testing for Huntington disease using the polymerase chain reaction;McIntosh, I.; Curtis, A.; Millan, F.A.; Brock, D.J.H.;Amj Med Genet,1989

4. The oculocerebrocutaneous (Delleman) syndrome;Al-Gazali, L.I.; Donnai, D.; Berry, S.A.; Say, B.; Mueller, R.F.;Med Genet,1988

5. Congenital mnicrophthalmos with cyst formation;Ladenheim, J.; Metrick, S.;Am Ophthalmol,1956

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1. An update on oculocerebrocutaneous (Delleman-Oorthuys) syndrome;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-12

2. Delleman syndrome: A case report from West Africa - features and the challenges of management;Nigerian Postgraduate Medical Journal;2018

3. Oral Mucosal Lesions of Systemic Diseases;Case Based Oral Mucosal Diseases;2018

4. Ossifying Fibroma in a Patient With Oculocerebrocutaneous (Delleman) Syndrome;Journal of Oral and Maxillofacial Surgery;2015-07

5. Delleman Oorthuys syndrome;Middle East African Journal of Ophthalmology;2015

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