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Author/Creator Barnett, Christopher P.

3. Cover Image, Volume 37, Issue 9. Issue 9 (September 2016)

Authors:
Barnett, Christopher P.; Nataren, Nathalie J.; Klingler‐Hoffmann, Manuela; Schwarz, Quenten; Chong, Chan‐Eng; Lee, Young K.; Bruno, Damien L.; Lipsett, Jill; McPhee, Andrew J.; Schreiber, Andreas W.; Feng, Jinghua; Hahn, Christopher N.; Scott, Hamish S.
Journal:
Human mutation
Issue:
Volume 37:Issue 9(2016)
Page Start:
i
Record Type:
Journal Article
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5. Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome Sequencing. Issue 9 (11th July 2016)

Authors:
Barnett, Christopher P.; Nataren, Nathalie J.; Klingler‐Hoffmann, Manuela; Schwarz, Quenten; Chong, Chan‐Eng; Lee, Young K.; Bruno, Damien L.; Lipsett, Jill; McPhee, Andrew J.; Schreiber, Andreas W.; Feng, Jinghua; Hahn, Christopher N.; Scott, Hamish S.
Journal:
Human mutation
Issue:
Volume 37:Issue 9(2016)
Page Start:
955
Record Type:
Journal Article
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6. Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System. Issue 11 (November 2020)

Authors:
Lunke, Sebastian; Eggers, Stefanie; Wilson, Meredith; Patel, Chirag; Barnett, Christopher P.; Pinner, Jason; Sandaradura, Sarah A.; Buckley, Michael F.; Krzesinski, Emma I.; de Silva, Michelle G.; Brett, Gemma R.; Boggs, Kirsten; Mowat, David; Kirk, Edwin P.; Adès, Lesley C.; Akesson, Lauren S.; ...
Journal:
Obstetrical & gynecological survey
Issue:
Volume 75:Issue 11(2020)
Page Start:
Record Type:
Journal Article
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7. Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate Families. Issue 7 (6th May 2016)

Authors:
McInerney‐Leo, Aideen M.; Harris, Jessica E.; Gattas, Michael; Peach, Elizabeth E.; Sinnott, Stephen; Dudding‐Byth, Tracy; Rajagopalan, Sulekha; Barnett, Christopher P.; Anderson, Lisa K.; Wheeler, Lawrie; Brown, Matthew A.; Leo, Paul J.; Wicking, Carol; Duncan, Emma L.
Journal:
Human mutation
Issue:
Volume 37:Issue 7(2016)
Page Start:
695
Record Type:
Journal Article
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8. Gene‐specific facial dysmorphism in Axenfeld‐Rieger syndrome caused by FOXC1 and PITX2 variants. Issue 2 (24th November 2020)

Authors:
Souzeau, Emmanuelle; Siggs, Owen M.; Pasutto, Francesca; Knight, Lachlan S. W.; Perez‐Jurado, Luis A.; McGregor, Lesley; Le Blanc, Shannon; Barnett, Christopher P.; Liebelt, Jan; Craig, Jamie E.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 2(2021)
Page Start:
434
Record Type:
Journal Article
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9. High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation. Issue 11 (21st August 2015)

Authors:
Rojnueangnit, Kitiwan; Xie, Jing; Gomes, Alicia; Sharp, Angela; Callens, Tom; Chen, Yunjia; Liu, Ying; Cochran, Meagan; Abbott, Mary‐Alice; Atkin, Joan; Babovic‐Vuksanovic, Dusica; Barnett, Christopher P.; Crenshaw, Melissa; Bartholomew, Dennis W.; Basel, Lina; Bellus, Gary; Ben‐Shachar, Shay; Bi...
Journal:
Human mutation
Issue:
Volume 36:Issue 11(2015:Nov.)
Page Start:
1052
Record Type:
Journal Article
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