33 documents found, page 1 of 4

Hyoid Bone Position and Head Posture in Patients With Richieri-Costa Pereira Sy...

Made available in DSpace on 2020-12-12T02:10:15Z (GMT). No. of bitstreams: 0 Previous issue date: 2020-06-01; Robin sequence with cleft mandible and limb anomalies, known as Richieri-Costa-Pereira syndrome (RCPS), is an autosomal recessive acrofacial dysostosis characterized by mandibular cleft and other craniofacial anomalies and respiratory complications. The aim of this cross-sectional study was to describe ...

Craniofacial Morphology in Patients With Opitz G/BBB Syndrome

Made available in DSpace on 2019-10-06T16:44:04Z (GMT). No. of bitstreams: 0 Previous issue date: 2019-01-01; Objective: To compare the cephalometric characteristics of patients with and without Opitz G/BBB syndrome type I. Design: Cross-sectional, case–control study. Setting: Tertiary cleft center in Brazil. Participants: Eighteen individuals with Opitz G/BBB syndrome with complete bilateral cleft lip and pala...

Fluency aspects of oral narrative task in del22q11.2 syndrome

Made available in DSpace on 2018-12-11T17:30:47Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-01-01. Added 1 bitstream(s) on 2019-10-09T18:32:45Z : No. of bitstreams: 1 S2317-17822016000400373.pdf: 853168 bytes, checksum: 61cff0db26918bc638615ba65b300b65 (MD5); Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq); Purpose: To investigate the fluency aspects of the oral narrative task in...

Language, behavior and neurodevelopment in Joubert syndrome: A case report

Made available in DSpace on 2018-12-11T17:30:49Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-01-01. Added 1 bitstream(s) on 2019-10-09T18:32:46Z : No. of bitstreams: 1 S2317-17822016000600823.pdf: 866087 bytes, checksum: 06d06c54144f4e3ed5228336cf8138db (MD5); The Joubert syndrome (JS) is a rare, heterogeneous genetic condition among the ciliopathies. More than 20 genes have been identified associated...

Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies,...

Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis

Radiological and CT scan evaluation of mandible and ear in 56 cases with oculoa...

Phenotypic evaluation and evolution in syndromic (SC) and non-syndromic cranios...

Frontonasal dysplasia: clinical evaluation on audiological and brainstem electr...

Made available in DSpace on 2015-03-19T16:20:28Z (GMT). No. of bitstreams: 0 Previous issue date: 2011-10-01Bitstream added on 2015-03-19T16:29:19Z : No. of bitstreams: 1 S1808-86942011000500013-pt.pdf: 297908 bytes, checksum: 97221b928877588e73e76830db1fab0e (MD5)Bitstream added on 2015-03-19T16:29:19Z : No. of bitstreams: 2 S1808-86942011000500013-pt.pdf: 297908 bytes, checksum: 97221b928877588e73e76830db1fab...

Achados audiológicos e eletrofisiológicos de indivíduos com a síndrome G/BBB

Submitted by Guilherme Lemeszenski (guilherme@nead.unesp.br) on 2013-08-22T18:44:21Z No. of bitstreams: 1 S1808-86942011000600014.pdf: 325926 bytes, checksum: 364d628b6b32341131295cb669cb15e3 (MD5); Made available in DSpace on 2013-08-22T18:44:21Z (GMT). No. of bitstreams: 1 S1808-86942011000600014.pdf: 325926 bytes, checksum: 364d628b6b32341131295cb669cb15e3 (MD5) Previous issue date: 2011-12-01; Made availabl...