Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes.
about
Conditions presenting with symptoms of peripheral arterial diseaseNovel Pathogenic Variant in TGFBR2 Confirmed by Molecular Modeling Is a Rare Cause of Loeys-Dietz Syndrome.Loeys-Dietz syndrome: a primer for diagnosis and management.RET is a potential tumor suppressor gene in colorectal cancer.Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlations.A rare cause of recurrent aortic dissection.A mutation update on the LDS associated genes TGFB2/3 and SMAD2/3.The new Ghent criteria for Marfan syndrome: what do they change?
P2860
Q30301251-A572BBEC-78F2-43EB-A320-14499FFC9502Q30398243-A1B9C0D5-D7F3-49D2-B8EA-F427A117A501Q34038144-78293A14-0501-40C7-93E6-2484D333818EQ36301488-79A0AA4A-769C-436F-B0F3-B2D32696D695Q36866985-4D33ED91-6B38-40B1-BC7A-947D26C6244AQ42562706-5FD2A284-A571-4537-9340-A29476ADDA89Q47824296-553A65A3-0A75-4B98-81F7-9C4ADC690E36Q49060891-21F7FDF7-9243-4C56-A9DE-98186C4F2D66
P2860
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes.
@en
type
label
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes.
@en
prefLabel
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes.
@en
P2093
P2860
P356
P1476
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes.
@en
P2093
Guillaume Jondeau
Jörg Schmidtke
Jörg T Epplen
Laurence Faivre
Mine Arslan-Kirchner
P2860
P2888
P304
P356
10.1038/EJHG.2011.68
P577
2011-04-27T00:00:00Z