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Author/Creator McMullan, Dominic J.

2. Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data. Issue 10 (29th July 2022)

Authors:
Hardcastle, Amy; Berry, Aliska M.; Campbell, Ian M.; Zhao, Xiaonan; Liu, Pengfei; Gerard, Amanda E.; Rosenfeld, Jill A.; Sisoudiya, Saumya D.; Hernandez‐Garcia, Andres; Loddo, Sara; Di Tommaso, Silvia; Novelli, Antonio; Dentici, Maria L.; Capolino, Rossella; Digilio, Maria C.; Graziani, Ludovico;...
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 10(2022)
Page Start:
2958
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Prenatal central nervous system anomaly with skeletal dysplasia associated with a de novo interstitial tandem triplication of chromosome 14. (3rd April 2017)

Authors:
Hall, Georgina K.; Mackie, Fiona L.; Williams, Helen; Williams, Denise; Cox, Phillip; McMullan, Dominic J.; Allen, Stephanie; Kilby, Mark D.
Journal:
Journal of obstetrics and gynaecology
Issue:
Volume 37:Number 3(2017)
Page Start:
375
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases. (22nd August 2019)

Authors:
Chong, Hsu P.; Hamilton, Susan; Mone, Fionnuala; Cheung, Ka Wang; Togneri, Fiona S.; Morris, Rachel K.; Quinlan‐Jones, Elizabeth; Williams, Denise; Allen, Stephanie; McMullan, Dominic J.; Kilby, Mark D.
Journal:
Prenatal diagnosis
Issue:
Volume 39:Number 12(2019)
Page Start:
1064
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗