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m6aViewer: software for the detection, analysis, and visualization of [electronic resource] by
- Antanaviciute, Agne
- Baquero-Perez, Belinda
- Watson, Christopher M
- Harrison, Sally M
- Lascelles, Carolina
- Crinnion, Laura
- Markham, Alexander F
- Bonthron, David T
- Whitehouse, Adrian
- Carr, Ian M
Producer: 20171019
In:
RNA (New York, N.Y.) vol. 23
Availability: No items available.
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11.
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Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping. [electronic resource] by
- Watson, Christopher M
- Crinnion, Laura A
- Berry, Ian R
- Harrison, Sally M
- Lascelles, Carolina
- Antanaviciute, Agne
- Charlton, Ruth S
- Dobbie, Angus
- Carr, Ian M
- Bonthron, David T
Producer: 20160511
In:
BMC medical genetics vol. 17
Availability: No items available.
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12.
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Novel avian paramyxovirus isolated from gulls in Caspian seashore in Kazakhstan. [electronic resource] by
- Karamendin, Kobey
- Kydyrmanov, Aidyn
- Kasymbekov, Yermukhammet
- Asanova, Saule
- Daulbayeva, Klara
- Seidalina, Aigerim
- Khan, Elizaveta
- Harrison, Sally M
- Carr, Ian M
- Goodman, Simon J
- Moldakozhayev, Alibek
- Sayatov, Marat
Producer: 20180215
In:
PloS one vol. 12
Availability: No items available.
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13.
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Deficiency of the myogenic factor MyoD causes a perinatally lethal fetal akinesia. [electronic resource] by
- Watson, Christopher M
- Crinnion, Laura A
- Murphy, Helen
- Newbould, Melanie
- Harrison, Sally M
- Lascelles, Carolina
- Antanaviciute, Agne
- Carr, Ian M
- Sheridan, Eamonn
- Bonthron, David T
- Smith, Audrey
Producer: 20161213
In:
Journal of medical genetics vol. 53
Availability: No items available.
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14.
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Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome. [electronic resource] by
- Watson, Christopher M
- Crinnion, Laura A
- Tzika, Antigoni
- Mills, Alison
- Coates, Andrea
- Pendlebury, Maria
- Hewitt, Sarah
- Harrison, Sally M
- Daly, Catherine
- Roberts, Paul
- Carr, Ian M
- Sheridan, Eamonn G
- Bonthron, David T
Producer: 20150604
In:
American journal of medical genetics. Part A vol. 164A
Availability: No items available.
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15.
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Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interface. [electronic resource] by
- Watson, Christopher M
- Crinnion, Laura A
- Morgan, Joanne E
- Harrison, Sally M
- Diggle, Christine P
- Adlard, Julian
- Lindsay, Helen A
- Camm, Nick
- Charlton, Ruth
- Sheridan, Eamonn
- Bonthron, David T
- Taylor, Graham R
- Carr, Ian M
Producer: 20150129
In:
Human mutation vol. 35
Availability: No items available.
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16.
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Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data. [electronic resource] by
- Carr, Ian M
- Morgan, Joanne
- Watson, Christopher
- Melnik, Svitlana
- Diggle, Christine P
- Logan, Clare V
- Harrison, Sally M
- Taylor, Graham R
- Pena, Sergio D J
- Markham, Alexander F
- Alkuraya, Fowzan S
- Black, Graeme C M
- Ali, Manir
- Bonthron, David T
Producer: 20140127
In:
Human mutation vol. 34
Availability: No items available.
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