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D J McMullan

Showing results (1-10 of 13) 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|August 14, 2012
Microarray comparative genomic hybridization in prenatal diagnosis: a reviewS C Hillman, D J McMullan, D Williams, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 23, 2013
How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings?S C Hillman, D J McMullan, L Silcock, et al.
Journal of Medical Genetics|April 1, 1995
Partial trisomy 22 (q11.2-q13.1) as a result of duplication and pericentric inversionV P Prasher, E Roberts, A Norman, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|February 16, 2021
Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies: Scientific Impact Paper No. 64 [February] 2021F Mone, D J McMullan, D Williams, et al.
Histopathology|February 21, 2006
Ewing's sarcoma of bone: the detection of specific transcripts in a large, consecutive series of formalin-fixed, decalcified, paraffin-embedded tissue samples using the reverse transcriptase-polymerase chain reactionD C Mangham, A Williams, D J McMullan, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 27, 2010
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysisS C Hillman, S Pretlove, A Coomarasamy, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 23, 2021
Evolving fetal phenotypes and clinical impact of progressive prenatal exome sequencing pathways: cohort studyF Mone, H Abu Subieh, S Doyle, et al.
Cancer Genetics and Cytogenetics|October 25, 2001
Molecular cytogenetic characterization of two non-MYCN amplified neuroblastoma cell lines with complex t(11;17)C M McConville, S Dyer, S A Rees, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 21, 2013
Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysisS C Hillman, D J McMullan, G Hall, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 11, 2020
COngenital heart disease and the Diagnostic yield with Exome sequencing (CODE) study: prospective cohort study and systematic reviewF Mone, R Y Eberhardt, R K Morris, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 14, 2012
Microarray comparative genomic hybridization in prenatal diagnosis: a reviewS C Hillman, D J McMullan, D Williams, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 23, 2013
How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings?S C Hillman, D J McMullan, L Silcock, et al.
Journal of Medical Genetics|April 1, 1995
Partial trisomy 22 (q11.2-q13.1) as a result of duplication and pericentric inversionV P Prasher, E Roberts, A Norman, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|February 16, 2021
Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies: Scientific Impact Paper No. 64 [February] 2021F Mone, D J McMullan, D Williams, et al.
Histopathology|February 21, 2006
Ewing's sarcoma of bone: the detection of specific transcripts in a large, consecutive series of formalin-fixed, decalcified, paraffin-embedded tissue samples using the reverse transcriptase-polymerase chain reactionD C Mangham, A Williams, D J McMullan, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 27, 2010
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysisS C Hillman, S Pretlove, A Coomarasamy, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 23, 2021
Evolving fetal phenotypes and clinical impact of progressive prenatal exome sequencing pathways: cohort studyF Mone, H Abu Subieh, S Doyle, et al.
Cancer Genetics and Cytogenetics|October 25, 2001
Molecular cytogenetic characterization of two non-MYCN amplified neuroblastoma cell lines with complex t(11;17)C M McConville, S Dyer, S A Rees, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 21, 2013
Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysisS C Hillman, D J McMullan, G Hall, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 11, 2020
COngenital heart disease and the Diagnostic yield with Exome sequencing (CODE) study: prospective cohort study and systematic reviewF Mone, R Y Eberhardt, R K Morris, et al.
Pageof 2