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Foresta C.
Foresta Carlo
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http://hub.abes.fr/bmj/periodical/jmedgenet/2007/volume_44/issue_3/B3598D6B63E67CBEE053120B220A90C5/authorship/10
http://hub.abes.fr/bmj/periodical/jmedgenet/2005/volume_42/issue_3/B3598D6B62497CBEE053120B220A90C5/authorship/8
http://hub.abes.fr/oup/periodical/molehr/2010/volume_16/issue_6/101093molehrgaq026/authorship/5
http://hub.abes.fr/oup/periodical/molehr/2006/volume_12/issue_6/101093molehrgal043/authorship/7
http://hub.abes.fr/oup/periodical/molehr/2004/volume_10/issue_4/101093molehrgah036/authorship/6
http://hub.abes.fr/oup/periodical/molehr/2007/volume_13/issue_9/101093molehrgam052/authorship/6
http://hub.abes.fr/oup/periodical/humrep/2008/volume_23/issue_8/101093humrepden193/authorship/9
http://hub.abes.fr/oup/periodical/humrep/2004/volume_19/issue_6/101093humrepdeh255/authorship/1
http://hub.abes.fr/oup/periodical/humrep/2008/volume_23/issue_4/101093humrepdem400/authorship/8
http://hub.abes.fr/oup/periodical/molehr/2004/volume_10/issue_8/101093molehrgah073/authorship/5
http://hub.abes.fr/oup/periodical/molehr/2004/volume_10/issue_6/101093molehrgah054/authorship/6
http://hub.abes.fr/oup/periodical/molehr/2010/volume_16/issue_6/101093molehrgaq015/authorship/6
http://hub.abes.fr/bmj/periodical/bmj/2009/volume_339/issue_2009/B36EB7A14E645E22E053120B220A683D/authorship/1
http://hub.abes.fr/bmj/periodical/jmedgenet/2003/volume_40/issue_1/B3598D6B5F4E7CBEE053120B220A90C5/authorship/5
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Y chromosome haplogroups and susceptibility to testicular cancer
Endothelial progenitor cells as a new cardiovascular risk factor in Klinefelter's syndrome
Characterization of HSFY, a novel AZFb gene on the Y chromosome with a possible role in human spermatogenesis
Suppression of the high endogenous levels of plasma FSH in infertile men are associated with improved Sertoli cell function as reflected by elevated levels of plasma inhibin B
A possible association of a human tektin-t gene mutation (A229V) with isolated non-syndromic asthenozoospermia: Case Report
Insulin-like factor 3 gene mutations in testicular dysgenesis syndrome: clinical and functional characterization
Lack of the T54A polymorphism of the DAZL gene in infertile Italian patients
Androgen receptor gene CAG and GGC repeat lengths in idiopathic male infertility
Osteoporosis in Klinefelter's syndrome
Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia
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