The BOR syndrome and renal agenesis-prenatal diagnosis andfurther clinical delineation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference7 articles.
1. Genetic aspects of the BOR syndrome—branchial fistulas, ear pits, hearing loss, and renal anomalies
2. Branchio-oto-renal syndrome: Reduced penetrance and variable expressivity in four generations of a large kindred
3. Branchio-oto-renal dysplasia and branchio-oto dysplasia: Two distinct autosomal dominant disorders
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1. Prenatal diagnosis and follow-up of a case of branchio-oto-renal syndrome displays renal growth impairment after the second trimester;Journal of Obstetrics and Gynaecology Research;2015-07-30
2. Deafness;Molecular Pathology in Clinical Practice: Genetics;2009
3. Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndrome;Clinical Genetics;2008-06-28
4. Deafness;Molecular Pathology in Clinical Practice;2007
5. Prenatal Sonographic Diagnosis of Major Craniofacial Anomalies;Plastic and Reconstructive Surgery;2001-10
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