机译：Ring chromosome 15 involving deletion of the insulinhyphen;like growth factor 1 receptor gene in a patient with features of Silverhyphen;Russell syndrome
机译：A case of lateral facial clefts with Fallot tetralogycomma; duodenal stenosis and intestinal malrotationa new multiple congenital anomaly syndromequest;
机译：Three mildly retarded siblings with congenital cataractscomma; sensorineural deafnesscomma; hypogonadismcomma; hypertrichosis and short staturea new syndromequest;
机译：Double dens invaginatus of molarized maxillary central incisorscomma; premolarization of maxillary lateral incisorscomma; multituberculism of the mandibular incisorscomma; canines and first premolarcomma; and sensorineural hearing loss
机译：Hemifacial microsomia, external auditory canal atresia, deafness and Mullerian anomalies associated with acro-osteolysiscolon; a new autosomal recessive syndrome?
