Ring chromosome 15 in a patient with features of Fryns' syndrome
about
Two fetuses with Fryns syndrome without diaphragmatic defectsVariability in the phenotypic expression of fryns syndrome: A report of two sibships.Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridizationFryns syndrome: a surviving case with associated Hirschsprung's disease and hemidiaphragmatic agenesis.Genetic factors in congenital diaphragmatic hernia.Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.Fryns syndrome: a new definition.Good growth response to growth hormone treatment in the ring chromosome 15 syndrome.Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature.Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.
P2860
Q33596333-6DC24E0C-E097-4CDE-9A05-30D0D361C242Q33930456-60B7316C-765A-4877-A585-403015BFB598Q33942314-05378237-E232-44FB-8457-C122B4F54CC8Q34669506-6B124D64-7976-4227-A9C0-AEDC62929EFCQ35752633-755AC7D9-3D73-4366-A7BB-8699E24F833DQ36493270-8A9BDC55-A098-4833-A7DC-69684B352EE6Q40692266-ED10E85B-C217-4374-87D1-2374786FE4F6Q41909566-68690625-DDA8-407B-8871-B26A01D12265Q46966456-FADB56B9-4CB1-4045-B252-98CF11F31D5AQ51960539-DA2F0481-E3F2-40A7-94A4-4219DF7519B6
P2860
Ring chromosome 15 in a patient with features of Fryns' syndrome
description
1989 nî lūn-bûn
@nan
1989 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Ring chromosome 15 in a patient with features of Fryns' syndrome
@ast
Ring chromosome 15 in a patient with features of Fryns' syndrome
@en
Ring chromosome 15 in a patient with features of Fryns' syndrome
@en-gb
Ring chromosome 15 in a patient with features of Fryns' syndrome
@nl
type
label
Ring chromosome 15 in a patient with features of Fryns' syndrome
@ast
Ring chromosome 15 in a patient with features of Fryns' syndrome
@en
Ring chromosome 15 in a patient with features of Fryns' syndrome
@en-gb
Ring chromosome 15 in a patient with features of Fryns' syndrome
@nl
prefLabel
Ring chromosome 15 in a patient with features of Fryns' syndrome
@ast
Ring chromosome 15 in a patient with features of Fryns' syndrome
@en
Ring chromosome 15 in a patient with features of Fryns' syndrome
@en-gb
Ring chromosome 15 in a patient with features of Fryns' syndrome
@nl
P2093
P356
P1476
Ring chromosome 15 in a patient with features of Fryns' syndrome
@en
P2093
A E Retief
R A Rossouw
P2860
P304
P356
10.1136/JMG.26.7.469
P407
P577
1989-07-01T00:00:00Z