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This page includes a sampling of up to 25 citations for "Genetic Testing in Children" from the last year of listings within the PubMed database. If these citations appear useful you may wish to run the search again at PubMed for a complete listing of all available citations.
PubMed is a service of the National Center for Biotechnology Information (NCBI), a division of the National Library of Medicine (NLM) at the National Institutes of Health (NIH). The NLM does not hold the copyright on abstracts that may be attached to PubMed entries; the copyright holders are the publishers of the journals in which the abstracts appear. Please read the NCBI Disclaimer and Copyright Notice before accessing material from PubMed.
Atypical presentations and specific genotypes are associated with a delay in diagnosis in females with Rett syndrome.
Am J Med Genet A
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Epigenetics, copy number variation, and other molecular mechanisms underlying neurodevelopmental disabilities: new insights and diagnostic approaches.
J Dev Behav Pediatr
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Carrier testing for spinal muscular atrophy.
Genet Med
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Voicing the lifeworld: Parental accounts of responsibility in genetic consultations for polycystic kidney disease.
Soc Sci Med
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What Were You Thinking?: Individuals at Risk for Huntington Disease Talk About Having Children.
J Genet Couns
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Evaluation of GPR50, hMel-1B, and ROR-alpha Melatonin-related Receptors and the Etiology of Adolescent Idiopathic Scoliosis.
J Pediatr Orthop
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Corrected QT Interval in Children With Brain Death.
Pediatr Cardiol
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Discussion of Morris and Jewell's editorial 'Array of hope for high-resolution genetic screening services in New Zealand'.
N Z Med J
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Genetic Polymorphisms in Adaptive Immunity Genes and Childhood Acute Lymphoblastic Leukemia.
Cancer Epidemiol Biomarkers Prev
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NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease.
J Pediatr Surg
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Cardiovascular manifestations in men and women carrying a FBN1 mutation.
Eur Heart J
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Genetics of Wilsons disease.
Parkinsonism Relat Disord
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Double-heterozygous mutations involving both HNF1A (MODY3) and HNF4A (MODY1) genes: a case report.
Diabetes Care
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Embryo aneuploidy and the role of morphological and genetic screening.
Reprod Biomed Online
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Agenesis of maxillary lateral incisors and associated dental anomalies.
Am J Orthod Dentofacial Orthop
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Neurobehavioral abnormalities in first-degree relatives of individuals with autism.
Arch Gen Psychiatry
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A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM).
Am J Obstet Gynecol
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Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome.
Am J Hum Genet
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Original research: parents and children with cystic fibrosis.
Am J Nurs
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Sensorineural hearing loss in children.
Ir Med J
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The role of disease perceptions and results sharing in psychological adaptation after genetic susceptibility testing: the REVEAL Study.
Eur J Hum Genet
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Update on emerging therapies for multiple sclerosis.
Expert Rev Neurother
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Genetic analyses of HIV-1 env sequences demonstrate limited compartmentalization in breast milk and suggest viral replication within the breast that increases with mastitis.
J Virol
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A hereditary moyamoya syndrome with multisystemic manifestations.
Neurology
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Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis.
Pediatrics
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