Shprintzen-Goldberg syndrome: a clinical analysis.

Shprintzen-Goldberg syndrome: a clinical analysis.

Item
http://www.wikidata.org/entity/Q41723685
Marfan's syndromeThe molecular genetics of Marfan syndrome and related microfibrillopathiesGuideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on CraniosynostosisIdentification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 geneConnective tissue disorders and cardiovascular complications: the indomitable role of transforming growth factor-beta signalingMutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysmMaxillofacial Changes in Melnick-Needles SyndromeShprintzen-Goldberg syndrome presenting as umbilical hernia in an Indian child.Shprintzen-Goldberg syndrome: a rare disorder.Shprintzen-Goldberg syndrome associated with a novel missense mutation in TGFBR2.Abnormal steroidogenesis in three patients with Antley-Bixler syndrome: apparent decreased activity of 17alpha-hydroxylase, 17,20-lyase and 21-hydroxylase
P2860

Shprintzen-Goldberg syndrome: a clinical analysis.

Item
http://www.wikidata.org/entity/Q41723685
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Shprintzen-Goldberg syndrome: a clinical analysis.
@en
type
label
Shprintzen-Goldberg syndrome: a clinical analysis.
@en
prefLabel
Shprintzen-Goldberg syndrome: a clinical analysis.
@en
P1433
P1476
P2093
P304
P31
P356
P433
P478
P577
P698
P356
P1433
P1476
Shprintzen-Goldberg syndrome: a clinical analysis.
@en
P2093
P304
P31
P356
10.1002/(SICI)1096-8628(19980319)76:3<202::AID-AJMG2>3.3.CO;2-Z
P433
P478
P577
P698