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2 results for author:"Backeljauw P.F." in Literature citations

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A molecular basis for variation in clinical severity of isolated growth hormone deficiency type II.

Hamid R., Phillips J.A., Holladay C., Cogan J.D., Austin E.D., Backeljauw P.F., Travers S.H., Patton J.G.

J. Clin. Endocrinol. Metab. 94:4728-4734(2009) · Mapped (7)

Homozygous deletion of the human insulin receptor gene results in leprechaunism.

Wertheimer E., Lu S.P., Backeljauw P.F., Davenport M.L., Taylor S.I.

Nat. Genet. 5:71-73(1993)

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