Antenatal diagnosis of CHARGE syndrome: Prenatal ultrasound findings and crucial role of fetal dysmorphic signs. About a series of 10 cases and review of literature
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference44 articles.
1. Ultrasound evaluation of development of olfactory sulci in normal fetuses: a possible role in diagnosis of CHARGE syndrome;Acanfora;Ultrasound Obstet. Gynecol.,2016
2. CHARGE Syndrome-a five case study of the syndrome characteristics and health care consumption during the first year in life;Anderzén-Carlsson;J. Pediatr. Nurs.,2015
3. MRI of the olfactory bulbs and sulci in human fetuses;Azoulay;Pediatr. Radiol.,2006
4. Reproductive endocrine phenotypes relating to CHD7 mutations in humans;Balasubramanian;Am J Med Genet C Semin Med Genet,2017
5. Prenatal detection of unilateral nasal airway obstruction caused by a dacryocystocele;Bardin;Ultrasound Obstet. Gynecol.,2016
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3. 3D ultrasound evaluation of fetal ears in prenatal syndrome diagnosis – a comparative study;Ultraschall in der Medizin - European Journal of Ultrasound;2024-01-25
4. Digenic CHD7 and SMCHD1 inheritance Unveils phenotypic variability in a family mainly presenting with hypogonadotropic hypogonadism;Heliyon;2024-01
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