نتایج جستجو برای: nonsyndromic

تعداد نتایج: 1750  

Journal: :Pakistan Journal of Medical and Health Sciences 2022

Background: Intellectual Disability “ID” is a genetic disorder, which lead to arrested or incomplete development of the brain. It limitation cognitive skills impairment and decline ability person in learning process. ID most common health problem worldwide. These patients have intellectual functions at least their two more adoptive such as reading, writing abilities, social interactions, Behavi...

Journal: :The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology 2005
Kristina Aldridge Alex A Kane Jeffrey L Marsh Jayesh Panchal Simeon A Boyadjiev Peng Yan Daniel Govier Warda Ahmad Joan T Richtsmeier

Studies of isolated craniosynostosis have shown biomechanical and biochemical influences on the craniofacial phenotype, resulting from both genetic and epigenetic factors. Much less attention has been directed toward the morphology of the brain, despite the interactive nature of the developing skull and developing brain. The aim of this study is to define the morphology of the brain in nonsyndr...

Journal: :Journal of biological regulators and homeostatic agents 2015
A A Chokoeva G Tchernev J W Patterson U Wollina T Lotti

Aplasia cutis congenita (ACC) is a rare disorder, which is defined by the localized, or less commonly widespread absence of skin involving the epidermis, dermis and subcutaneous tissue with an incidence of 1/10.000 newborns. The underlying bone and dura mater can be also affected, and muscle and bone involvement occur in approximately 20 to 30% of the cases. Aplasia cutis congenita most often o...

Journal: :Journal of Pharmacy and Bioallied Sciences 2014

Journal: :Archives of Otolaryngology–Head & Neck Surgery 1998

Journal: :International Archives of Otorhinolaryngology 2014

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