Template:Genetic risk maternal age table: Difference between revisions
From Embryology
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! width=200px|<center>Risk of {{trisomy 21}}</center> | ! width=200px|<center>Risk of {{trisomy 21}}</center> | ||
! width=200px|<center>Risk of Any Chromosomal Abnormality</center> | ! width=200px|<center>Risk of Any Chromosomal Abnormality</center> | ||
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| <center>20</center> | | <center>20</center> | ||
| <center>1 in 1667</center> | | <center>1 in 1667</center> |
Revision as of 13:14, 18 April 2018
Table Data[1][2][3] | ||
- ↑ Hook EB. (1981). Rates of chromosome abnormalities at different maternal ages. Obstet Gynecol , 58, 282-5. PMID: 6455611
- ↑ Hook EB, Cross PK & Schreinemachers DM. (1983). Chromosomal abnormality rates at amniocentesis and in live-born infants. JAMA , 249, 2034-8. PMID: 6220164
- ↑ Schreinemachers DM, Cross PK & Hook EB. (1982). Rates of trisomies 21, 18, 13 and other chromosome abnormalities in about 20 000 prenatal studies compared with estimated rates in live births. Hum. Genet. , 61, 318-24. PMID: 6891368