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Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss. Mol Cytogenet 2015;8:18.
. Population genetic differentiation of height and body mass index across Europe. Nat Genet 2015;47(11):1357-62.
. Population genetic differentiation of height and body mass index across Europe. Nat Genet 2015;47(11):1357-62.
. PRE- AND POSTNATAL MODIFICATIONS IN PARENTAL MENTAL REPRESENTATIONS IN THREE CASES OF FETAL GASTROSCHISIS DIAGNOSED DURING PREGNANCY. Infant Ment Health J 2015;
. Prevalence of celiac disease in patients with severe food allergy. Allergy 2015;70(10):1346-9.
. Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015;6:7756.
. Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015;6:7756.
. Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015;6:7756.
. Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015;6:7756.
. Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015;6:7756.
. Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015;6:7756.
. Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015;6:7756.
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