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Hereditary Renal Cell Carcinoma Syndromes Clinical, Pathologic, and Genetic Features
Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2
Here's to the Losers: Evolvable Residents Accelerate the Evolution of High-Fitness Invaders
Hereditary angioedema: Special consideration in children, women of childbearing age, and the elderly
Hereditary angioedema in Medellin (Colombia): Clinical evaluation and quality of life appraisal
Hereditary breast cancer: an update on risk assessment and genetic testing in 2015
Hereditary spastic paraplegia SPG4: what is known and not known about the disease
Here today, gone tomorrow: Short-term retention of pesticide-induced tolerance in amphibians
Hereditary Gingivo-Alveolar Hyperplasia: A Report of Two Siblings
Hereditary motor and sensory neuropathies: Understanding molecular pathogenesis could lead to future treatment strategies
Hereditary spastic paraplegia-linked REEP1 modulates endoplasmic reticulum/mitochondria contacts
Here today, gone tomorrow: declines and local extinctions of invasive ant populations in the absence of intervention
Hereditary hyperparathyroidism-a consensus report of the European Society of Endocrine Surgeons (ESES)
Hereditary Ovarian Cancer: Not Only BRCA 1 and 2 Genes
Hereditary geniospasm in a Korean family
Here Comes the Sun-Is Vitamin D a Cure For All That Ails Us?
Hereditary and Common Familial Colorectal Cancer: Evidence for Colorectal Screening
何人绘得萧红影?——传记文学中对萧红形象的解读
Heredity of nasal polyps
Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease
Hereditary spherocytosis in a patient undergoing coronary artery bypass grafting with cardiopulmonary bypass - a case report
Hereditary haemochromatosis caused by homozygous HJV mutation evolved through paternal disomy
Hereditary angioedema with a focus on the child
Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload
Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis
Here comes the sun: the era of genetics
Hereditary gingival fibromatosis: Clinical and ultrastructural features of a new family
Hereditary Spherocytosis in a Middle-aged Man Complicated with Common Bile Duct Stones
Hereditary Spherocytosis. Review. Part II. Symptomatology, outcome, complications, and treatment
Hereditary epidermolysis bullosa
Hereditary and Clinical Features of Retinitis Pigmentosa in Koreans
Hereditary Behavior of Varicocele
Hereditary Non-polyposis Colorectal Cancer/Lynch Syndrome in Korean Patients with Endometrial Cancer
Hereditary Angioedema - Therapies Old and New
Hereditary myeloproliferative disorders
Hereditary thrombocytosis not as innocent as thought? Development into acute leukemia and myelofibrosis
Heredity and Predictive Testing of Alcoholism: An Exploratory Study of the Views of Dutch Alcoholics, At-Risk Drinkers, and Health Care Providers
Hereditary causes of kidney tumours
Hereditary muscular dystrophies and the heart
Hereditary and acquired protein S deficiencies are associated with low TFPI levels in plasma
Hereditary motor and sensory neuropathy type 4A
Hereditary Palmoplantar Keratoderma and Deafness Resulting from Genetic Mutation of Connexin 26
Hereditary Breast-Ovarian Cancer Syndrome in Russia
Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations
Hereditary haemorrhagic telangiectasia Pathophysiology, diagnosis and treatment
Hereditary fibrinogen A alpha-chain amyloidosis: phenotypic characterization of a systemic disease and the role of liver transplantation
Hereditary haemorrhagic telangiectasia and genetic thrombophilia Reply
Hereditary and acquired thrombotic risk factors for chronic thromboembolic pulmonary hypertension
Hereditary haemorrhagic telangiectasia: From symptomatic management to pathogenesis based treatment Reply
Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19
Hereditary fibrinogen A alpha-chain amyloidosis: clinical phenotype and role of liver transplantation
Hereditary Sensory Neuropathy Type 1 Is Caused by the Accumulation of Two Neurotoxic Sphingolipids
Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation
Hereditary Hemorrhagic Telangiectasia/Avastin
Hereditary Multiple Exostoses With Spine Involvement in a 4-Year-Old Boy
Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects
Hereditary disorders of renal phosphate wasting
Hereditary Cerebellar Degeneration in Scottish Terriers