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Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism. [electronic resource] by
- Johnson, S R
- Leo, P J
- McInerney-Leo, A M
- Anderson, L K
- Marshall, M
- McGown, I
- Newell, F
- Brown, M A
- Conwell, L S
- Harris, M
- Duncan, E L
Producer: 20190212
In:
Pediatric diabetes vol. 19
Availability: No items available.
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5.
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Point mutation in p14 [electronic resource] by
- McInerney-Leo, A M
- Wheeler, L
- Sturm, R A
- Tan, J-M
- Harris, J E
- Anderson, L
- Jagirdar, K
- Brown, M A
- Leo, P J
- Soyer, H P
- Duncan, E L
Producer: 20190913
In:
The British journal of dermatology vol. 178
Availability: No items available.
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The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls. [electronic resource] by
- McMeniman, E K
- Duffy, D L
- Jagirdar, K
- Lee, K J
- Peach, E
- McInerney-Leo, A M
- De'Ambrosis, B
- Rayner, J E
- Smithers, B M
- Soyer, H P
- Sturm, R A
Producer: 20210514
In:
The British journal of dermatology vol. 183
Availability: No items available.
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7.
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Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophies. [electronic resource] by
- McInerney-Leo, A M
- Harris, J E
- Leo, P J
- Marshall, M S
- Gardiner, B
- Kinning, E
- Leong, H Y
- McKenzie, F
- Ong, W P
- Vodopiutz, J
- Wicking, C
- Brown, M A
- Zankl, A
- Duncan, E L
Producer: 20160831
In:
Clinical genetics vol. 88
Availability: No items available.
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