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6 results for author:"Cisternino M." in Literature citations

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Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations.

Longoni M., Moncini S., Cisternino M., Morella I.M., Ferraiuolo S., Russo S., Mannarino S., Brazzelli V., Coi P., Zippel R. et al.

Am. J. Med. Genet. A 152:2176-2184(2010) · UniProtKB (2) · Mapped (6)

A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure.

Corre T., Schuettler J., Bione S., Marozzi A., Persani L., Rossetti R., Torricelli F., Giotti I., Vogt P., Toniolo D. et al.

Hum. Reprod. 24:2023-2028(2009) · Mapped (1)

Genetic analysis and evaluation of resistance to thyrotropin and growth hormone-releasing hormone in pseudohypoparathyroidism type Ib.

Mantovani G., Bondioni S., Linglart A., Maghnie M., Cisternino M., Corbetta S., Lania A.G., Beck-Peccoz P., Spada A.

J. Clin. Endocrinol. Metab. 92:3738-3742(2007) · Mapped (12)

Helicobacter pylori infection and autoimmune thyroid disease in young patients: the disadvantage of carrying the human leukocyte antigen-DRB1*0301 allele.

Larizza D., Calcaterra V., Martinetti M., Negrini R., De Silvestri A., Cisternino M., Iannone A.M., Solcia E.

J. Clin. Endocrinol. Metab. 91:176-179(2006) · Mapped (306)

The acid-labile subunit of human ternary insulin-like growth factor-binding protein complex in girls with central precocious puberty before and during gonadotropin-releasing hormone analog therapy.

Cisternino M., Draghi M., Lauriola S., Scarcella D., Bernasconi S., Cavallo L., De Luca F., Lomeo A., Tato L.

J. Clin. Endocrinol. Metab. 87:4629-4633(2002) · Mapped (3)

Two novel SRY missense mutations reducing DNA binding identified in XY females and their mosaic fathers.

Schmitt-Ney M., Thiele H., Kaltwasser P., Bardoni B., Cisternino M., Scherer G.

Am. J. Hum. Genet. 56:862-869(1995) · UniProtKB (1)

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