Pages that link to "Q37826266"
Jump to navigation
Jump to search
The following pages link to Array technology in prenatal diagnosis. (Q37826266):
Displaying 11 items.
- Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 (Q27004138) (← links)
- Rapid aneuploidy detection or karyotyping? Ethical reflection (Q35304082) (← links)
- Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature (Q35839324) (← links)
- Women's experiences receiving abnormal prenatal chromosomal microarray testing results (Q37424832) (← links)
- Patient preferences for prenatal testing of microdeletion and microduplication syndromes (Q40188449) (← links)
- Informed Decision-Making in the Context of Prenatal Chromosomal Microarray (Q50420407) (← links)
- Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization (Q50856798) (← links)
- Counseling parents before prenatal diagnosis: do we need to say more about the sex chromosome aneuploidies? (Q53087139) (← links)
- The introduction of arrays in prenatal diagnosis: a special challenge. (Q53131950) (← links)
- Microarrays as a diagnostic tool in prenatal screening strategies: ethical reflection (Q58663048) (← links)
- 0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practice (Q86794263) (← links)