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Screening and Diagnosis Research

Antenatal detection of Edwards (Trisomy 18) and Patau (Trisomy 13) syndrome: England and Wales 2005-2012.

Springett AL, Morris JK (2014) J Med Screen. 21(3): 113-9


Prenatal counseling and parental decision-making following a fetal diagnosis of trisomy 13 or 18

Winn P, Acharya K, Peterson E, Leuthner S (2018) J Perinatol. 38: 788-96



Using Patient-Centered Care After a Prenatal Diagnosis of Trisomy 18 or Trisomy 13: A Review

Haug S, Goldstein M; Cummins D, Fayard E, Merritt A (2017) JAMA Pediatr. 171(4): 382-7




Obstetric practice patterns in pregnancies complicated by fetal trisomy 13 or 18

Dotters-Katz SK, Smid MC, Mcelwain C, Kuller JA, Schulkin J (2018) J Matern Fetal Neonatal Med. 31(18): 2441-5


Revised estimates of the risk of fetal loss following a prenatal diagnosis of trisomy 13 or trisomy 18

Cavadino A, Morris JK (2017) Am J Med Genet. 173(4): 953-8



The National Down Syndrome Cytogenetic Register for England and Wales: 2013 Annual Report

Morris JK, Springett A (2014)




National Congenital Anomaly and Rare Disease Registration Service: Congenital anomaly statistics 2017 Public Health England (2019)

Congenital Anomalies Surveillance 2013-2014: Review of Data Relating to Congenital Anomalies Detected in NHS GG&C between 1st April 2013 and 31st March 2014.

Robins J (2014) NHS Greater Glasgow & Clyde.




Congenital Anomalies Surveillance 2015-2016: Reivew of Data relating to Congenital Anomalies Detected in NHS GG&C Between 1st April 2015 and 31st March 2016.

Robins J (2016) NHS Greater Glasgow & Clyde 


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