Clinical Significance of the Parental Origin of the X Chromosome in Turner Syndrome | Zendy

Liora Sagi | Zendy; Nehama ZuckermanLevin | Zendy; Aneta Gawlik | Zendy; Lucia Ghizzoni | Zendy; Atilla Büyükgebiz | Zendy; Yardena Rakover | Zendy; T. Bistritzer | Zendy; Osnat Admoni | Zendy; Alessandra Vottero | Zendy; Oshrat Baruch | Zendy; Fuad Fares | Zendy; Ewa MałeckaTendera | Zendy; Ze’ev Hochberg | Zendy

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Clinical Significance of the Parental Origin of the X Chromosome in Turner Syndrome

Author(s) -

Liora Sagi,

Nehama ZuckermanLevin,

Aneta Gawlik,

Lucia Ghizzoni,

Atilla Büyükgebiz,

Yardena Rakover,

T. Bistritzer,

Osnat Admoni,

Alessandra Vottero,

Oshrat Baruch,

Fuad Fares,

Ewa MałeckaTendera,

Ze’ev Hochberg

Publication year - 2006

Publication title -

the journal of clinical endocrinology and metabolism

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.206

H-Index - 353

eISSN - 1945-7197

pISSN - 0021-972X

DOI - 10.1210/jc.2006-0158

Subject(s) - turner syndrome , x chromosome , karyotype , biology , genetics , y chromosome , chromosome , phenotype , endocrinology , medicine , gene

The phenotype in Turner syndrome (TS) is variable, even in patients with a supposedly nonmosaic karyotype. Previous work suggested that there were X-linked parent-of-origin effects on the phenotype.

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