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Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate. [electronic resource] by
- Downey, Louise M
- Keen, T Jeffrey
- Jalili, Ismail K
- McHale, John
- Aldred, Michael J
- Robertson, Steven P
- Mighell, Alan
- Fayle, Steven
- Wissinger, Bernd
- Inglehearn, Chris F
Producer: 20030826
In:
European journal of human genetics : EJHG vol. 10
Availability: No items available.
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15.
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Oral focal mucinosis: report of 15 cases and review of the literature. [electronic resource] by
- Aldred, Michael J
- Talacko, Anna A
- Ruljancich, Kevin
- Story, Rowan D
- Newland, Stuart
- Chen, Stephen T
- O'Grady, John F
- Bergman, John D
- Smith, Andrew
- Dimitroulis, George
- Redman, John
- Sheldon, William R
- Mansour, Alan K
- Watkins, Don
- Radden, Bryan G
Producer: 20040129
In:
Pathology vol. 35
Availability: No items available.
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16.
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Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta. [electronic resource] by
- Parry, David A
- Brookes, Steven J
- Logan, Clare V
- Poulter, James A
- El-Sayed, Walid
- Al-Bahlani, Suhaila
- Al Harasi, Sharifa
- Sayed, Jihad
- Raïf, El Mostafa
- Shore, Roger C
- Dashash, Mayssoon
- Barron, Martin
- Morgan, Joanne E
- Carr, Ian M
- Taylor, Graham R
- Johnson, Colin A
- Aldred, Michael J
- Dixon, Michael J
- Wright, J Tim
- Kirkham, Jennifer
- Inglehearn, Chris F
- Mighell, Alan J
Producer: 20121217
In:
American journal of human genetics vol. 91
Availability: No items available.
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