id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_kf2xw7mkxzel7e4hjza7kmyybi	Timothy D. Howard	Autosomal Dominant Postaxial Polydactyly, Nail Dystrophy, and Dental Abnormalities Map to Chromosome 4p16, in the Region Containing the Ellis–van Creveld Syndrome Locus	1997.0	8	.pdf	application/pdf	5266	570	63	Weyers acrofacial dysostosis is an autosomal dominant condition with dental anomalies, nail (oral frenula), dental abnormalities (neonatal teeth, hypodontia, and premature tooth loss), cardiac malformations (atrial septal defect and single atrium), genitourinary anomalies (epispadias and hypospadias), limbs are similar in Ellis–van Creveld and Jeune syndromes, but nail dystrophy, abnormal frenula, and cardiac abnormalities are not found in the latter condition. dominant form of postaxial polydactyly type A to chromosome 7p15-q11.23 recently was reported in a fivegeneration Indian family with no other clinical findings the autosomal dominant mild short stature, four-extremity postaxial polydactyly type A, onychodystrophy, hypodontia, and abnormal frenula, with which the affected The proband in this family has features most consistent with Ellis–van Creveld syndrome. a condition with features of both Weyers acrofacial dysostosis and Ellis–van Creveld syndrome. Autosomal Dominant Postaxial Polydactyly, Nail Dystrophy, and Dental Abnormalities Map to Chromosome 4p16, in the Region Containing the Ellis–van Creveld Syndrome Locus	./cache/work_kf2xw7mkxzel7e4hjza7kmyybi.pdf	./txt/work_kf2xw7mkxzel7e4hjza7kmyybi.txt