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Items: 3

1.

A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome.

Risheg H, Graham JM Jr, Clark RD, Rogers RC, Opitz JM, Moeschler JB, Peiffer AP, May M, Joseph SM, Jones JR, Stevenson RE, Schwartz CE, Friez MJ.

Nat Genet. 2007 Apr;39(4):451-3. Epub 2007 Mar 4.

PMID:
17334363
2.

Further evidence for the role of genes on chromosome 2 and chromosome 5 in the inheritance of pulmonary function.

Malhotra A, Peiffer AP, Ryujin DT, Elsner T, Kanner RE, Leppert MF, Hasstedt SJ.

Am J Respir Crit Care Med. 2003 Sep 1;168(5):556-61. Epub 2003 Jun 5.

PMID:
12791583
3.

Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p.

Drayna D, Coon H, Kim UK, Elsner T, Cromer K, Otterud B, Baird L, Peiffer AP, Leppert M; Utah Genetic Reference Project.

Hum Genet. 2003 May;112(5-6):567-72. Epub 2003 Mar 6.

PMID:
12624758

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