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D Chitayat

Showing results (121-130 of 211) with videos related to

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 18, 2006
Fetal cardiac calcifications: report of four prenatally diagnosed cases and review of the literatureM J Simchen, A Toi, M Silver, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 19, 2004
Caroli's disease: prenatal diagnosis, postnatal outcome and genetic analysisM Sgro, S Rossetti, T Barozzino, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 16, 1998
Gonadoblastoid testicular dysplasia in Walker-Warburg syndromeN A Hung, M M Silver, D Chitayat, et al.
European Journal of Medical Genetics|May 29, 2016
Analysis of tissue from products of conception and perinatal losses using QF-PCR and microarray: A three-year retrospective study resulting in an efficient protocolK Wou, Y Hyun, D Chitayat, et al.
Journal of Medical Genetics|June 19, 2002
Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in CanadaJ S Waye, L M Nakamura, B Eng, et al.
American Journal of Medical Genetics|October 1, 1991
Syndrome of mental retardation and distal arthrogryposis in sibsD Chitayat, K A Hodgkinson, S Blaichman, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 23, 2019
Microarray and RASopathy-disorder testing in fetuses with increased nuchal translucencyP Sinajon, D Chitayat, M Roifman, et al.
Clinical Genetics|May 28, 2014
Fetal skeletal dysplasias in a tertiary care center: radiology, pathology, and molecular analysis of 112 casesE Barkova, U Mohan, D Chitayat, et al.
Clinical Genetics|April 5, 2014
Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 geneS Moalem, P Brouillard, D Kuypers, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Elevation of serum beta-hexosaminidase and alpha-D-mannosidase in type 2 Gaucher disease: a clinical and biochemical studyD Chitayat, S Nakagawa, R W Marion, et al.
Pageof 22

Showing results (121-130 of 211) with videos related to

Sort By:
Pageof 22
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 18, 2006
Fetal cardiac calcifications: report of four prenatally diagnosed cases and review of the literatureM J Simchen, A Toi, M Silver, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 19, 2004
Caroli's disease: prenatal diagnosis, postnatal outcome and genetic analysisM Sgro, S Rossetti, T Barozzino, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 16, 1998
Gonadoblastoid testicular dysplasia in Walker-Warburg syndromeN A Hung, M M Silver, D Chitayat, et al.
European Journal of Medical Genetics|May 29, 2016
Analysis of tissue from products of conception and perinatal losses using QF-PCR and microarray: A three-year retrospective study resulting in an efficient protocolK Wou, Y Hyun, D Chitayat, et al.
Journal of Medical Genetics|June 19, 2002
Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in CanadaJ S Waye, L M Nakamura, B Eng, et al.
American Journal of Medical Genetics|October 1, 1991
Syndrome of mental retardation and distal arthrogryposis in sibsD Chitayat, K A Hodgkinson, S Blaichman, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 23, 2019
Microarray and RASopathy-disorder testing in fetuses with increased nuchal translucencyP Sinajon, D Chitayat, M Roifman, et al.
Clinical Genetics|May 28, 2014
Fetal skeletal dysplasias in a tertiary care center: radiology, pathology, and molecular analysis of 112 casesE Barkova, U Mohan, D Chitayat, et al.
Clinical Genetics|April 5, 2014
Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 geneS Moalem, P Brouillard, D Kuypers, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Elevation of serum beta-hexosaminidase and alpha-D-mannosidase in type 2 Gaucher disease: a clinical and biochemical studyD Chitayat, S Nakagawa, R W Marion, et al.
Pageof 22