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IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families. [electronic resource] by
- Leslie, E J
- Koboldt, D C
- Kang, C J
- Ma, L
- Hecht, J T
- Wehby, G L
- Christensen, K
- Czeizel, A E
- Deleyiannis, F W-B
- Fulton, R S
- Wilson, R K
- Beaty, T H
- Schutte, B C
- Murray, J C
- Marazita, M L
Producer: 20170522
In:
Clinical genetics vol. 90
Availability: No items available.
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A polymorphism in the VKORC1 regulator calumenin predicts higher warfarin dose requirements in African Americans. [electronic resource] by
- Voora, D
- Koboldt, D C
- King, C R
- Lenzini, P A
- Eby, C S
- Porche-Sorbet, R
- Deych, E
- Crankshaw, M
- Milligan, P E
- McLeod, H L
- Patel, S R
- Cavallari, L H
- Ridker, P M
- Grice, G R
- Miller, R D
- Gage, B F
Producer: 20100416
In:
Clinical pharmacology and therapeutics vol. 87
Availability: No items available.
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The Alzheimer's Disease Sequencing Project: Study design and sample selection. [electronic resource] by
- Beecham, Gary W
- Bis, J C
- Martin, E R
- Choi, S-H
- DeStefano, A L
- van Duijn, C M
- Fornage, M
- Gabriel, S B
- Koboldt, D C
- Larson, D E
- Naj, A C
- Psaty, B M
- Salerno, W
- Bush, W S
- Foroud, T M
- Wijsman, E
- Farrer, L A
- Goate, A
- Haines, J L
- Pericak-Vance, Margaret A
- Boerwinkle, E
- Mayeux, R
- Seshadri, S
- Schellenberg, G
Publication details: Neurology. Genetics Oct 2017
In:
Neurology. Genetics vol. 3
Availability: No items available.
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