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Works matching IS 1178704X AND DT 2008 AND VI 1

Results: 3

1

Greig cephalopolysyndactyly (GCPS) contiguous gene syndrome in a boy with a 14 Mb deletion in region 7p13-14 caused by a paternal balanced insertion (5; 7).

Published in:

Application of Clinical Genetics, 2008, v. 1, p. 19

By:

Schulz, Solveig;
Volleth, Marianne;
Muschke, Petra;
Wieland, Ilse;
Wieacker, Peter

Publication type:

Article

2

A comparison of the genetic and clinical profile of men that respond and do not respond to the immediate antihypertensive effects of aerobic exercise.

Published in:

Application of Clinical Genetics, 2008, v. 1, p. 7

By:

Pescatello, Linda S.;
Blanchard, Bruce E.;
Tsongalis, Gregory J.;
O'Connell, Ann A.;
Gordish-Dressman, Heather;
Maresh, Carl M.;
Thompson, Paul D.

Publication type:

Article

3

Hemodialysis for hyperammonemia associated with ornithine transcarbamylase deficiency.

Published in:

Application of Clinical Genetics, 2008, v. 1, p. 1

By:

Collen, Jacob F.;
Das, Nealanjon P.;
Koff, Jonathan M.;
Neff, Robert T.;
Abbott, Kevin C.

Publication type:

Article