The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

P Jay, C Rougeulle, A Massacrier, A Moncla… - Nature …, 1997 - nature.com
Prader-Willi syndrome (PWS) is a neurogenetic disorder that results from the absence of a
normal paternal contribution to the 15q11–13 region1–3. The clinical manifestations of PWS …
被引用次数：287 相关文章

[引用][C] The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

P Jay, C Rougeulle, A Massacrier, A Moncla… - Nature …, 1997 - cnrs.hal.science
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi
syndrome chromosomal region - CNRS - Centre national de la recherche scientifique …

[引用][C] The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

P Jay, C Rougeulle, A Massacrier, A Moncla… - Nature Genetics, 1997 - cir.nii.ac.jp
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi
syndrome chromosomal region | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region.

P Jay, C Rougeulle, A Massacrier, A Moncla… - Nature …, 1997 - europepmc.org
Prader-Willi syndrome (PWS) is a neurogenetic disorder that results from the absence of a
normal paternal contribution to the 15q11-13 region. The clinical manifestations of PWS are …

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

P Jay, C Rougeulle, A Massacrier… - Nature …, 1997 - pubmed.ncbi.nlm.nih.gov
Prader-Willi syndrome (PWS) is a neurogenetic disorder that results from the absence of a
normal paternal contribution to the 15q11-13 region. The clinical manifestations of PWS are …

[引用][C] The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

P Jay, C Rougeulle, A Massacrier, A Moncla… - Nature Genetics, 1997 - hal.science
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome
chromosomal region - Archive ouverte HAL Accéder directement au contenu Opérations de …

[引用][C] The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

P JAY, C ROUGEULLE, P BERTA… - Nature …, 1997 - pascal-francis.inist.fr
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi
syndrome chromosomal region CNRS Inist Pascal-Francis CNRS Pascal and Francis …

[引用][C] The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

P JAY - Nat. Genet, 1997 - cir.nii.ac.jp
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi
syndrome chromosomal region | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …

[引用][C] The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

P JAY, C ROUGEULLE, A MASSACRIER… - Nature …, 1997 - Nature Publishing Group