| Table of Contents, Volume 175C, Number 4, December 2017 |
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| Publication schedule for 2017 |
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| Cover Image, Volume 175C, Number 4, December 2017 |
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| Phenotype and genotype analysis of a French cohort of 119 patients with CHARGE syndrome |
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| Distinct cerebellar foliation anomalies in a <i>CHD7</i> haploinsufficient mouse model of CHARGE syndrome |
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| Guidelines in CHARGE syndrome and the missing link: Cranial imaging |
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| New insights and advances in CHARGE syndrome: Diagnosis, etiologies, treatments, and research discoveries |
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| Reproductive endocrine phenotypes relating to <i>CHD7</i> mutations in humans |
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| Immunodeficiency in CHARGE syndrome |
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| Genetic counseling in CHARGE syndrome: Diagnostic evaluation through follow up |
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| Clinical and molecular effects of <i>CHD7</i> in the heart |
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| CHARGEd with neural crest defects |
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| Gastrointestinal and feeding difficulties in CHARGE syndrome: A review from head‐to‐toe |
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| Inner ear manifestations in CHARGE: Abnormalities, treatments, animal models, and progress toward treatments in auditory and vestibular structures |
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| Behavior in CHARGE syndrome |
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| Publication schedule for 2017 |
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| Cover Image, Volume 175C, Number 3, September 2017 |
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| Genetic rodent models of brain disorders: Perspectives on experimental approaches and therapeutic strategies |
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| Table of Contents, Volume 175C, Number 3, September 2017 |
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| Microstructural white matter tract alteration in Prader‐Willi syndrome: A diffusion tensor imaging study |
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| Irving Gottesman and the concept of endophenotype |
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| Phenotypes, pleiotropy, and phylogeny |
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| Whither the genotype‐phenotype relationship? An historical and methodological appraisal |
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| Introduction to behavioral phenotypes in medical genetics |
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| Phenotype analysis of congenital and neurodevelopmental disorders in the next generation sequencing era |
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| Similar reliability and equivalent performance of female and male mice in the open field and water‐maze place navigation task |
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| A review of endophenotypes in schizophrenia and autism: The next phase for understanding genetic etiologies |
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| Cover Image, Volume 175C, Number 2, June 2017 |
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| Table of Contents, Volume 175C, Number 2, June 2017 |
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| Publication schedule for 2017 |
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| Challenges in educating patients and parents about differences in sex development |
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| Emerging issues in disorders/differences of sex development (DSD) |
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| Interdisciplinary care in disorders/differences of sex development (DSD): The psychosocial component of the DSD—Translational research network |
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| Disorders of sex development (DSD): Clinical service delivery in the United States |
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| Gynecological challenges in the diagnosis and care of patients with DSD: The role of the obstetrician gynecologist in the multidisciplinary approach to the patient |
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| Unexpected ethical dilemmas in sex assignment in 46,XY DSD due to 5‐alpha reductase type 2 deficiency |
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| A practical guide for evaluating gonadal germ cell tumor predisposition in differences of sex development |
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| <i>MAP3K1</i>‐related gonadal dysgenesis: Six new cases and review of the literature |
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| Table of Contents, Volume 175C, Number 1, March 2017 |
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| Publication schedule for 2017 |
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| The evidence‐based rationale for physical therapy treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome |
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| The international consortium on the Ehlers–Danlos syndromes |
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| Cover Image, Volume 175C, Number 1, March 2017 |
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| Measurement properties of clinical assessment methods for classifying generalized joint hypermobility—A systematic review |
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| The Ehlers–Danlos syndromes, rare types |
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| The 2017 international classification of the Ehlers–Danlos syndromes |
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| Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome |
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| Mast cell disorders in Ehlers–Danlos syndrome |
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| Neurological and spinal manifestations of the Ehlers–Danlos syndromes |
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| Oral and mandibular manifestations in the Ehlers–Danlos syndromes |
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| Orthopaedic management of the Ehlers–Danlos syndromes |
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| Ehlers–Danlos syndrome, classical type |
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| Gastrointestinal involvement in the Ehlers–Danlos syndromes |
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| Chronic fatigue in Ehlers–Danlos syndrome—Hypermobile type |
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| Psychiatric and psychological aspects in the Ehlers–Danlos syndromes |
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| Pain management in the Ehlers–Danlos syndromes |
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| Cardiovascular autonomic dysfunction in Ehlers–Danlos syndrome—Hypermobile type |
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| Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history |
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| A framework for the classification of joint hypermobility and related conditions |
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