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Archives of Neurology|May 1, 1989
Joubert's syndrome associated with congenital ocular fibrosis and histidinemiaR E Appleton, D Chitayat, J E Jan, et al.
American Journal of Medical Genetics|August 26, 1998
Clustering of FBN2 mutations in patients with congenital contractural arachnodactyly indicates an important role of the domains encoded by exons 24 through 34 during human developmentE S Park, E A Putnam, D Chitayat, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 4, 2014
Beals syndrome (congenital contractural arachnodactyly): prenatal ultrasound findings and molecular analysisM Inbar-Feigenberg, N Meirowitz, D Nanda, et al.
Clinical Genetics|May 1, 1987
Partial duplication 16q: report of two affected siblings resulting from a maternal translocation and literature reviewS Y Hahm, D Chitayat, M A Iqbal, et al.
Prenatal Diagnosis|July 28, 2010
The role of molecular microsatellite identity testing to detect sampling errors in prenatal diagnosisE J T Winsor, H Akoury, D Chitayat, et al.
Fetal Diagnosis and Therapy|December 1, 2006
Prenatal diagnosis of fetal exencephaly associated with amniotic band sequence at 17 weeks of gestation by fetal magnetic resonance imagingM Rohrbach, D Chitayat, J Drake, et al.
The British Journal of Radiology|December 16, 2014
Foetal "black bone" MRI: utility in assessment of the foetal spineA J Robinson, S Blaser, A Vladimirov, et al.
American Journal of Medical Genetics. Part A|March 29, 2005
Functional disomy of Xp: prenatal findings and postnatal outcomeE Kolomietz, K Godbole, E J T Winsor, et al.
American Journal of Medical Genetics|June 1, 1992
Ring chromosome 20 and possible assignment of the structural gene encoding human carboxypeptidase-L to the distal segment of the long arm of chromosome 20F Halal, D Chitayat, H Parikh, et al.
Prenatal Diagnosis|May 18, 1999
Congenital toxoplasmosis: prenatal diagnosis, treatment and postnatal outcomeS Friedman, L E Ford-Jones, A Toi, et al.
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