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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 5, 2014
Genome-wide normalized score: a novel algorithm to detect fetal trisomy 21 during non-invasive prenatal testing
C H Yeang, G C Ma, H W Hsu, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 20, 2016
Detection of 22q11.2 microduplication by cell-free DNA screening and chromosomal microarray in fetus with multiple anomalies
W-J Wu, G-C Ma, Y-S Lin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 18, 2011
Experimental treatment of bilateral fetal chylothorax using in-utero pleurodesis
Y-S Yang, G-C Ma, J-C Shih, et al.
Lymphology
|
November 26, 2009
Genetic evaluation and management of fetal chylothorax: review and insights from a case of Noonan syndrome
C H Chen, T H Chen, S J Kuo, et al.
Genomics
|
December 1, 1996
A 1.5-megabase physical map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13
T F Wood, E S Srivatsan, R Chakrabarti, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
July 6, 2013
Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization
M Chen, Y-S Yang, J-C Shih, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 26) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 26 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 5, 2014
Genome-wide normalized score: a novel algorithm to detect fetal trisomy 21 during non-invasive prenatal testing
C H Yeang, G C Ma, H W Hsu, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 20, 2016
Detection of 22q11.2 microduplication by cell-free DNA screening and chromosomal microarray in fetus with multiple anomalies
W-J Wu, G-C Ma, Y-S Lin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 18, 2011
Experimental treatment of bilateral fetal chylothorax using in-utero pleurodesis
Y-S Yang, G-C Ma, J-C Shih, et al.
Lymphology
|
November 26, 2009
Genetic evaluation and management of fetal chylothorax: review and insights from a case of Noonan syndrome
C H Chen, T H Chen, S J Kuo, et al.
Genomics
|
December 1, 1996
A 1.5-megabase physical map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13
T F Wood, E S Srivatsan, R Chakrabarti, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
July 6, 2013
Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization
M Chen, Y-S Yang, J-C Shih, et al.
Page
of 3