Non-invasive screening of fragile X syndrome A using urine and hair roots

スポンサーリンク

概要

論文の詳細を見る
2004-09-15

著者

関連論文

Diagnosis of Arteriovenous Malformation of the Internal Iliac Vessels by Color Doppler Ultrasonography : A Case Report
Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boy
Elevated CSF IL-6 in a patient with respiratory syncytial virus encephalopathy
特発性ステロイド感受性ネフローゼ症候群にMIP-1βとIL-8は関与する
Volume measurement of a pediatric ventricular phantom model using three-dimensional echocardiography
Volume Measurement of Small Ventricular Model by Real-time Three-dimensional Echocardiography
Efficacy of Iodine-123-15-(p-iodophenyl)-3-R, S-Methylpentadecanoic Acid Single Photon Emission Computed Tomography Imaging in Detecting Myocardial Ischemia in Children With Kawasaki Disease
Inhalation of nebulized nitroglycerin in dogs with experimental pulmonary hypertension induced by U46619
Progressive Infundibular Stenosis after Balloon Pulmonary Valvuloplasty in Pulmonary Atresia with Intact Ventricular Septum in An Infant Who Underwent Brock Operation
Sequential Interventional Cardiac Catheterization Treatment of Combined Coarctation of the Aorta and Patent Ductus Arteriosus
Analysis of the intensity of radio-frequency signals in intracranial ultrasonography of preterm infants
新生児慢性肺疾患発症への Ureaplasma の関与
Autonomic Function in Adolescents with Orthostatic Dysregulation Measured by Heart Rate Variability
Autonomic function in Kawasaki disease with myocardial infarction : Usefulness of monitoring heart rate variability
Expression analysis and mutation detection of DLX5 and DLX6 in autism
Non-invasive screening of fragile X syndrome A using urine and hair roots
Case of Kawasaki disease in NICU
Unilaterally and rapidly progressing white matter lesion and elevated cytokines in a patient with Tay-Sachs disease
Mutation analysis of methyl-CpG binding protein family genes in autistic patients
Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients
RSK2 gene mutations in Coffin-Lowry syndrome with drop episodes
Association of autism in two patients with hereditary multiple exostoses caused by novel deletion mutations of EXT1
Change of specific T cells in an emerging neonatal infectious disease induced by a bacterial superantigen
Three-dimensional Echoencephalography in Infants
Simultaneous Measurement of Velocity Curves : Carotid Artery and Middle Cerebral Artery in Neonates
Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with nemaline myopathy
Serial Ultrasonographic Observations of Cerebral Ventricular Size in Pre-term Infants
Dichloroacetate treatment for mitochondrial cytopathy : long-term effects in MELAS
Transient cheiro-oral syndrome due to a ruptured intracranial dermoid cyst
早産児の慢性肺疾患発症と臍帯血 IL-8、Ureaplasma 保菌
Case of transient erythroblastopenia of childhood with transient hypogammaglobulinemia
Pseudotumor cerebri manifesting as a symptom of acute promyelocytic leukemia
A rare case of congenital hepatic fibrosis with severe pulmonary hypertension in an adolescent
Acute disseminated encephalomyelitis after live rubella vaccination
Th2 cells predominate in idiopathic steroid-sensitive nephrotic syndrome
Six-year-old girl with primary cutaneous aggressive epidermotropic CD8^+ T-cell lymphoma
Cytokine profile of a premature infant with early onset listeriosis
Another promising treatment option for neuroblastoma-associated opsoclonus-myoclonus syndrome by oral high-dose dexamethasone pulse : Lymphocyte markers as disease activity
Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination
The expression of retinoic acid receptor in the chick limb bud during early developmental stages.
The expression of cellular retinoic acid binding protein (CRABP) in the neural tube and notochord of mouse embryo.

もっと見る

スポンサーリンク