Skip to content
Welcome to University of UNSW, Bengaluru
Home
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文（繁體）
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
Māori
Sign In
全文检索
题名
作者
主题
索引号
ISBN/ISSN
标签
检索
高级检索
Channels
Newborn Screening in Japan
搜索更多频道:
相似书籍: Newborn Screening in Japan
Channel Options
View Record
探索相关频道
Quick Look
Newborn Screening for Congenital Hypothyroidism
Quick Look
Thyroid Disorders
Quick Look
The Unusual Presentation of Thyroid Disorders
Quick Look
Effects of Iodine Intake on Human Health
Quick Look
Homeostasis and Allostasis of Thyroid Function
Quick Look
Neonatal Screening for Critical Congenital Heart Defects
Quick Look
70 Years of Levothyroxine
Quick Look
Media Gizi Mikro Indonesia
Quick Look
Cryptorchidism: Causes and Consequences
Quick Look
CJC Pediatric and Congenital Heart Disease
Quick Look
Combination Therapy for Hypothyroidism
Quick Look
Advances in Research on Down Syndrome
Quick Look
Parasites and Infection
Quick Look
Journal of Clinical Orthopaedics
Quick Look
Novel Methods of Diagnostics of Thyroid and Parathyroid Lesions
Quick Look
Thyroid Disease
Quick Look
Risk Stratification of Thyroid Nodule: From Ultrasound Features to TIRADS
Quick Look
Minimal Access Cardiac Surgery
Quick Look
Down Syndrome
Quick Look
Hearing Disorders: Diagnosis, Management, and Future Opportunities
Quick Look
Pediatric Intensive Care
Quick Look
Клиническая и экспериментальная тиреоидология
Quick Look
Hearts
Quick Look
Zebrafish
Load more items
主题: homocystinuria
像这样添加更多频道
Toggle additional channel list for 主题: homocystinuria
主题: newborn screening
主题: long-term outcome
主题: social outcome
主题: vitamin B6
主题: methionine
主题: phenylketonuria
主题: hyperphenylalaninemia
主题: phenylalanine hydroxylase
主题: genetic analysis
主题: neonatal screening
主题: genotype–phenotype correlation
主题: adult patients
主题: Japanese
主题: intellectual disability
主题: psychiatric disability
主题: treatment discontinuation
主题: congenital hypothyroidism
主题: Japan
主题: re-evaluations
主题: prevalence
主题: lowering of thyroid stimulating hormone screening cutoffs
主题: thyroid dysgenesis
主题: thyroid dyshormonogenesis
主题: transient congenital hypothyroidism
主题: permanent congenital hypothyroidism
主题: delayed rise in TSH
主题: low birth weight
主题: propionic acidemia
主题: tandem mass spectrometry
主题: propionylcarnitine
主题: cardiomyopathy
主题: QT prolongation
主题: congenital adrenal hyperplasia
主题: 21-hydroxylase deficiency
主题: methylmalonic acidemia
主题: disorders of cobalamin metabolism
主题: hypomethioninemia
主题: isomer
主题: stable-isotope dilution
主题: derivatization
主题: cobalamin
主题: biotin
主题: maternal 3-methylcronylglycinuria
主题: argininosuccinic acid
主题: spinal muscular atrophy
主题: SMN1
主题: deletion
主题: incidence
主题: peroxisomal disorders
主题: adrenoleukodystrophy
主题: very-long-chain fatty acids
主题: plasmalogen
主题: phytanic acid
主题: presymptomatic diagnosis
主题: ABCD1
主题: whole-exome sequencing
主题: dried blood spot
主题: galactosemia
主题: GALM
主题: GALM deficiency
主题: glycogen storage disease type 1a
主题: allele-specific PCR
主题: mCOP-PCR
主题: melting curve
主题: n/a
主题: thema EDItEUR::M Medicine and Nursing
Channel Options
将项目显示为搜索结果
探索相关频道
Quick Look
Newborn Screening in Japan
Load more items
主题: cystathionine β-synthase deficiency
像这样添加更多频道
Toggle additional channel list for 主题: cystathionine β-synthase deficiency
主题: newborn screening
主题: long-term outcome
主题: social outcome
主题: vitamin B6
主题: methionine
主题: phenylketonuria
主题: hyperphenylalaninemia
主题: phenylalanine hydroxylase
主题: genetic analysis
主题: neonatal screening
主题: genotype–phenotype correlation
主题: adult patients
主题: Japanese
主题: intellectual disability
主题: psychiatric disability
主题: treatment discontinuation
主题: congenital hypothyroidism
主题: Japan
主题: re-evaluations
主题: prevalence
主题: lowering of thyroid stimulating hormone screening cutoffs
主题: thyroid dysgenesis
主题: thyroid dyshormonogenesis
主题: transient congenital hypothyroidism
主题: permanent congenital hypothyroidism
主题: delayed rise in TSH
主题: low birth weight
主题: propionic acidemia
主题: tandem mass spectrometry
主题: propionylcarnitine
主题: cardiomyopathy
主题: QT prolongation
主题: congenital adrenal hyperplasia
主题: 21-hydroxylase deficiency
主题: methylmalonic acidemia
主题: disorders of cobalamin metabolism
主题: hypomethioninemia
主题: isomer
主题: stable-isotope dilution
主题: derivatization
主题: cobalamin
主题: biotin
主题: maternal 3-methylcronylglycinuria
主题: argininosuccinic acid
主题: spinal muscular atrophy
主题: SMN1
主题: deletion
主题: incidence
主题: peroxisomal disorders
主题: adrenoleukodystrophy
主题: very-long-chain fatty acids
主题: plasmalogen
主题: phytanic acid
主题: presymptomatic diagnosis
主题: ABCD1
主题: whole-exome sequencing
主题: dried blood spot
主题: galactosemia
主题: GALM
主题: GALM deficiency
主题: glycogen storage disease type 1a
主题: allele-specific PCR
主题: mCOP-PCR
主题: melting curve
主题: n/a
主题: thema EDItEUR::M Medicine and Nursing
Channel Options
将项目显示为搜索结果
探索相关频道
Quick Look
Newborn Screening in Japan
Load more items
View Record
前一个
探索相关频道
下一个
