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Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2

Location: BCRP-Fac Medicina Rib Preto
Call Number: pcd 1682900
Status: On Shelf
Barcode: 11200052621-S
Item Type: DOCUMENTO IMPRESSO
Item Status: Referência - não circula
Copy Number: 1

A. P. Abreu E. B Trarbach; Margaret de Castro; E. M. F Costa; B Versiani; G Guerra Júnior; M. T. M Baptista; H. M Garmes; Berenice Bilharinho de Mendonça; A. C Latronico; Annual Meeting of the Endocrine Society (90. 2008 San Francisco)

Program and Abstracts Book San Francisco, 2008

Available at FMRP - Fac. Medicina de Ribeirão Preto (pcd 1682900 ) and other locations(GetIt)

FMRP - Fac. Medicina de Ribeirão Preto (pcd 1682900 ) Available

Location	Call Number	Description	Status	Barcode	Item Type	Request Options
BCRP-Fac Medicina Rib Preto	pcd 1682900		On Shelf	11200052621-S	DOCUMENTO IMPRESSO	Select Request Option: Click here to sign in
Location: BCRP-Fac Medicina Rib Preto Call Number: pcd 1682900 Status: On Shelf Barcode: 11200052621-S Item Type: DOCUMENTO IMPRESSO Item Status: Referência - não circula Copy Number: 1

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