The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology

Presentation information

APPES/JSPE Joint Session(English)

APPES/JSPE Joint Session(English) » Tea Break&Poster Discussion

P1-3: Pituitary & Others (CCS, dyslipidemia, etc)

Fri. Nov 18, 2016 2:45 PM - 3:35 PM Poster & Exhibition Room (Hall B5)

[P1-3-9] X chromosomal deletion due to microhomology-mediated break-induced replication in a boy with Xp22.3 contiguous gene deletion syndrome: Implications for novel genomic defects leading to Kallmann Syndrome

Koki Nagai1,2, Hirohito Shima1,3, Miki Kamimura3, Junko Kanno3, Ikuma Fujiwara4, Erina Suzuki1, Satoshi Narumi1, Akira Ishiguro2, Maki Fukami1 (1.Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 2.Department of Postgraduate Education and Training, National Center for Child Health and Development, 3.Department of Pediatrics, Tohoku University School of Medicine, 4.Department of Pediatric Endocrinology and Environmental Medicine, Tohoku University Graduate School of Medicine)

The password will be announced in the abstract book.

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