Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction
M Tauber, C Hoybye - The Lancet Diabetes & Endocrinology, 2021 - thelancet.com
Prader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting from the loss
of expression of maternally imprinted genes located in the paternal chromosomal region …
of expression of maternally imprinted genes located in the paternal chromosomal region …
Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction
M Tauber, C Hoybye - The lancet. Diabetes & …, 2021 - pubmed.ncbi.nlm.nih.gov
Prader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting from the loss
of expression of maternally imprinted genes located in the paternal chromosomal region …
of expression of maternally imprinted genes located in the paternal chromosomal region …
Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction
M Tauber, C Hoybye - The Lancet Diabetes & Endocrinology, 2021 - Elsevier
Prader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting from the loss
of expression of maternally imprinted genes located in the paternal chromosomal region …
of expression of maternally imprinted genes located in the paternal chromosomal region …
Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction.
M Tauber, C Hoybye - The lancet. Diabetes & Endocrinology, 2021 - europepmc.org
Prader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting from the loss
of expression of maternally imprinted genes located in the paternal chromosomal region …
of expression of maternally imprinted genes located in the paternal chromosomal region …
[引用][C] Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction
M Tauber, C Hoybye - The Lancet Diabetes & Endocrinology, 2021 - cir.nii.ac.jp
Endocrine disorders in Prader-Willi syndrome: a model to understand and treat
hypothalamic dysfunction | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …
hypothalamic dysfunction | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …
Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction
M Tauber, C Hoybye - The Lancet. Diabetes & …, 2021 - ut3-toulouseinp.hal.science
Prader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting from the loss
of expression of maternally imprinted genes located in the paternal chromosomal region …
of expression of maternally imprinted genes located in the paternal chromosomal region …