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2016 ◽  
Vol 47 (2) ◽  
pp. 177-183 ◽  
Author(s):  
S. J. Gross ◽  
M. Stosic ◽  
D. M. McDonald‐McGinn ◽  
A. S. Bassett ◽  
A. Norvez ◽  
...  
Keyword(s):  
Single Nucleotide Polymorphism ◽  
Clinical Experience ◽  
Prenatal Screening ◽  
22Q11.2 Deletion Syndrome ◽  
Deletion Syndrome ◽  
Nucleotide Polymorphism ◽  
22Q11.2 Deletion ◽  
Single Nucleotide ◽  
Non Invasive

Prenatal Diagnosis of 8p23 Deletion Syndrome by Single Nucleotide Polymorphism Microarray

2021 ◽  
Author(s):  
Didem Kaymak ◽  
Verda Alpay ◽  
Zafer Başıbüyük ◽  
Ebru Alıcı Davutoğlu ◽  
Riza Madazlı
Keyword(s):  
Single Nucleotide Polymorphism ◽  
Prenatal Diagnosis ◽  
Deletion Syndrome ◽  
Nucleotide Polymorphism ◽  
Single Nucleotide

scholarly journals Prenatal screening of DiGeorge (22q11.2 deletion) syndrome by abnormalities of the great arteries among Thai pregnant women

2020 ◽  
Vol 63 (3) ◽  
pp. 330-336
Author(s):  
Kuntharee Traisrisilp ◽  
Fuanglada Tongprasert ◽  
Kasemsri Srisupundit ◽  
Suchaya Luewan ◽  
Theera Tongsong
Keyword(s):  
Pregnant Women ◽  
Prenatal Screening ◽  
22Q11.2 Deletion Syndrome ◽  
Deletion Syndrome ◽  
22Q11.2 Deletion
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