[HTML] europepmc.org

[HTML][HTML] Beckwith-wiedemann syndrome

2016 - europepmc.org
Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably characterized by
neonatal hypoglycemia, macrosomia, macroglossia, hemihyperplasia, omphalocele …
被引用次数：239 相关文章
[HTML] nih.gov

[HTML][HTML] Beckwith-Wiedemann Syndrome

C Shuman, JM Kalish, R Weksberg - GeneReviews®[Internet], 2023 - ncbi.nlm.nih.gov
Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably characterized by
macroglossia, hemihyperplasia, omphalocele, neonatal hypoglycemia, macrosomia …
[HTML] europepmc.org

[HTML][HTML] Beckwith-Wiedemann Syndrome

C Shuman, JM Kalish, R Weksberg - 2016 - europepmc.org
Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably characterized by
macroglossia, hemihyperplasia, omphalocele, neonatal hypoglycemia, macrosomia …

[引用][C] Beckwith-Wiedemann syndrome

C SHUMAN - … at GeneTests: Medical Genetics Information Resource, 2005 - cir.nii.ac.jp
Beckwith-Wiedemann syndrome | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ
[サイニィ] 詳細へ移動 検索フォームへ移動 論文・データをさがす 大学図書館の本をさがす 日本の博士 …

Beckwith-Wiedemann Syndrome

C Shuman, JM Kalish… - GeneReviews® …, 1993 - pubmed.ncbi.nlm.nih.gov
Clinical characteristics Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably
characterized by macroglossia, hemihyperplasia, omphalocele, neonatal hypoglycemia …
[HTML] nih.gov

[HTML][HTML] Beckwith-Wiedemann Syndrome

C Shuman, JM Kalish, R Weksberg - GeneReviews®[Internet], 2023 - ncbi.nlm.nih.gov
Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably characterized by
macroglossia, hemihyperplasia, omphalocele, neonatal hypoglycemia, macrosomia …