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  1. 1101
    “…Sensory-motor axonal neuropathy and necklace fibres in biopsy were the major features expanding the phenotypic spectrum of SBF1-related recessive syndromic neuropathy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-020-09827-y) contains supplementary material, which is available to authorized users.…”
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    A novel frameshift deletion in autosomal recessive SBF1-related syndromic neuropathy with necklace fibres
  2. 1102
    “…To compare the surgical outcomes of medial rectus advancement and lateral rectus recession in postoperative consecutive exotropia with single-stage adjustable suture surgery. …”
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    Comparison of surgical outcomes between lateral rectus recession and medial rectus advancement for postoperative consecutive exotropia
  3. 1103
    “…We also find evidence that family provides a risk-sharing mechanism for recession graduates. Our results suggest that labor market entry in a large-scale recession has prolonged effects on a young worker’s life course even after the penalties in the labor market have disappeared.…”
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    The long-term effects of labor market entry in a recession: Evidence from the Asian financial crisis()
  4. 1104
    “…BACKGROUND: Both de novo variants and recessive inherited variants were associated with autism spectrum disorder (ASD). …”
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    Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder
  5. 1105
    “…Recessive dystrophic epidermolysis bullosa (RDEB) is a severe skin disease caused by mutation of the COL7A1 gene. …”
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    Raloxifene and n-Acetylcysteine Ameliorate TGF-Signalling in Fibroblasts from Patients with Recessive Dominant Epidermolysis Bullosa
  6. 1106
    “…Parkin-type autosomal recessive juvenile-onset Parkinson’s disease is caused by mutations in the PRKN gene and accounts for 50% of all autosomal recessive Parkinsonism cases. …”
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    A Splice Intervention Therapy for Autosomal Recessive Juvenile Parkinson’s Disease Arising from Parkin Mutations
  7. 1107
    “…An unavoidable consequence of periodontal flap procedure is gingival recession (GR). Achieving both pocket depth reduction and GR coverage remains a challenge to periodontists. …”
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    Semilunar Papilla Preservation Flap Technique in Combination with Chorion Membrane for Pocket Reduction and Gingival Recession Coverage
  8. 1108
    “…CONCLUSIONS: Ireland’s recent economic recession was accompanied by an overall decrease in the number of women choosing private maternity care after 2009. …”
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    Trends in private maternity care in Ireland’s capital during and after the Great Economic Recession 2009–2017
  9. 1109
    por Jiang, Peng, Ye, Cheng
    Publicado 2020
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    Recession of Environmental Barrier Coatings under High-Temperature Water Vapour Conditions: A Theoretical Model
  10. 1110
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    Retinal Pigment Epithelium Atrophy in Recessive Stargardt Disease as Measured by Short-Wavelength and Near-Infrared Autofluorescence
  11. 1111
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    Autosomal recessive variants in TUBGCP2 alter the γ-tubulin ring complex leading to neurodevelopmental disease
  12. 1112
    “…Interest in analyzing physically active behaviors during school recesses has grown in recent years as the school environment has consolidated (recess, physical education classes, lunch-time, before and after school) as a crucial space to bring these levels towards those recommended through intervention programs and improvements in the school environment. …”
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    Evidence-Based Overview of Accelerometer-Measured Physical Activity during School Recess: An Updated Systematic Review
  13. 1113
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    Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy
  14. 1114
    “…RESULTS: In a cohort of 3881 Brown Swiss bulls that had genotypes at 683,609 SNPs, we reveal four novel recessive QTL for male fertility on BTA1, 18, 25, and 26 using haplotype-based association testing. …”
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    Autosomal recessive loci contribute significantly to quantitative variation of male fertility in a dairy cattle population
  15. 1115
    “…The mutations in two GJB2 and GJB6 (Gap Junction Protein Beta 2, 6) genes are responsible for nearly 50% of autosomal recessive nonsyndromic hearing loss. The aim of the present study was to evaluate polymorphisms of 111C>T (rs7329857) and 337G>T (rs7333214) in GJB2 (encoding connexin 26) and GJB6 (encoding connexin 32) genes, respectively. …”
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    Evaluation of the GJB2 and GJB6 Polymorphisms with Autosomal Recessive Nonsyndromic Hearing Loss in Iranian Population
  16. 1116
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    Recessive COL4A2 Mutation Leads to Intellectual Disability, Epilepsy, and Spastic Cerebral Palsy
  17. 1117
    “…We report a consanguineous family in which schizophrenia segregates in a manner consistent with recessive inheritance of a rare, partial-penetrance susceptibility allele. …”
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    A Recessively Inherited Risk Locus on Chromosome 13q22-31 Conferring Susceptibility to Schizophrenia
  18. 1118
    Publicado 2021
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    From Clinical Phenotype to Genotypic Modelling: Incidence and Prevalence of Recessive Dystrophic Epidermolysis Bullosa (RDEB) [Corrigendum]
  19. 1119
    “…CONCLUSION: Properly planned changes in lower incisor and canine inclination can be carried out in adult patients without posing a high risk to labial gingival recessions if the individual periodontal biotype is respected. …”
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    Postorthodontic lower incisor and canine inclination and labial gingival recession in adult patients: A prospective study
  20. 1120
    “…Autosomal recessive cerebellar ataxias (ARCAs) form an ultrarare yet expanding group of neurodegenerative multisystemic diseases affecting the cerebellum and other neurological or non-neurological systems. …”
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    The ARCA Registry: A Collaborative Global Platform for Advancing Trial Readiness in Autosomal Recessive Cerebellar Ataxias
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