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Abnormal Auditory Brainstem Response (ABR) Findings in a Near-Normal Hearing Child with Noonan Syndrome.Clues in diagnosing congenital heart diseaseGenital tract function in men with Noonan syndrome.Noonan syndrome: clinical aspects and molecular pathogenesis.Growth and pubertal development in five boys with Noonan's syndrome.Paternal germline origin and sex-ratio distortion in transmission of PTPN11 mutations in Noonan syndrome.Severe pulmonary hypertension in Ullrich-Noonan syndrome.The dysplastic pulmonary valve: echocardiographic features and results of balloon dilatation.Turner Syndrome Genotype and phenotype and their effect on presenting features and timing of DiagnosisDisorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanismsPTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneityNoonan syndrome and clinically related disorders.Comprehensive massive parallel DNA sequencing strategy for the genetic diagnosis of the neuro-cardio-facio-cutaneous syndromes.Short stature in Noonan syndrome: response to growth hormone therapy.Clinical manifestations of Noonan syndrome.Clinical and molecular aspects of an informative family with neurofibromatosis type 1 and Noonan phenotype.A clinical study of Noonan syndrome.Bone resorption in syndromes of the Ras/MAPK pathway.PTPN11-associated mutations in the heart: has LEOPARD changed Its RASpots?Five-year response to growth hormone in children with Noonan syndrome and growth hormone deficiency.A novel approach to the analysis of human growth.Increased BRAF heterodimerization is the common pathogenic mechanism for noonan syndrome-associated RAF1 mutantsCerebral arteriovenous malformation in Noonan's syndrome.Cardiovascular malformations in Turner's and Noonan's syndromeNeurofibromatosis Type 1 Associated with Hashimoto's Thyroiditis: Coincidence or Possible LinkFunctional evaluation of circulating hematopoietic progenitors in Noonan syndromePragmatic language impairment in children with Noonan syndrome.Diagnosis of Noonan syndrome and related disorders using target next generation sequencing.Validation of auxological reference values for Japanese children with Noonan syndrome and comparison with growth in children with Turner syndrome.Asymmetric septal hypertrophy and propranolol treatment in a case of Ullrich-Noonan syndrome.Noonan syndrome: comparing mutation-positive with mutation-negative dutch patientsDevelopment of disease-specific growth charts in Turner syndrome and Noonan syndrome.
P2860
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P2860
description
1974 nî lūn-bûn
@nan
1974 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1974 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1974年の論文
@ja
1974年論文
@yue
1974年論文
@zh-hant
1974年論文
@zh-hk
1974年論文
@zh-mo
1974年論文
@zh-tw
1974年论文
@wuu
name
The Ullrich-Noonan syndrome (Turner phenotype).
@ast
The Ullrich-Noonan syndrome (Turner phenotype).
@en
The Ullrich-Noonan syndrome
@nl
type
label
The Ullrich-Noonan syndrome (Turner phenotype).
@ast
The Ullrich-Noonan syndrome (Turner phenotype).
@en
The Ullrich-Noonan syndrome
@nl
prefLabel
The Ullrich-Noonan syndrome (Turner phenotype).
@ast
The Ullrich-Noonan syndrome (Turner phenotype).
@en
The Ullrich-Noonan syndrome
@nl
P2093
P1476
The Ullrich-Noonan syndrome (Turner phenotype).
@en
P2093
P577
1974-01-01T00:00:00Z