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  1. 1181
    “…BACKGROUND/OBJECTIVE: The aim of this study was to examine the effects of school-based intervention integrating physical literacy (PL) into active school recesses (ASR) on physical fitness (i.e., body composition, 20-m shuttle run, 50-m run, rope skipping, sit and reach, handgrip) and academic achievement (i.e., academic result of Chinese and Mathematics) in Chinese children. …”
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    Effects of intervention integrating physical literacy into active school recesses on physical fitness and academic achievement in Chinese children
  2. 1182
    “…This is a report of a DGKG‐related recessive inherited disorder in cattle and adds DGKG to the list of candidate genes for HFSD in other species.…”
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    A missense variant in DGKG as a recessive functional variant for hepatic fibrinogen storage disease in Wagyu cattle
  3. 1183
    por Seashore, Margretta R.
    Publicado 1991
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    Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes. 9th Edition
  4. 1184
    por Seashore, Margretta R.
    Publicado 1987
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    Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes. 7th Edition
  5. 1185
    por Ellison, Viola, Stillman, Bruce
    Publicado 2003
    “…RSR preferred DNA substrates possessing 5′ recessed ends whereas RFC preferred 3′ recessed end DNA substrates. …”
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    Biochemical Characterization of DNA Damage Checkpoint Complexes: Clamp Loader and Clamp Complexes with Specificity for 5′ Recessed DNA
  6. 1186
    por Chun, Ko-i, Rah, Sang-hoon
    Publicado 2008
    “…RESULTS: In group A, BLR recessions was performed at the first surgery and BLR re-recession was performed at the second surgery. …”
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    The Comparision of Outcomes Between Lateral Rectus Muscles Re-recession and Medial Rectus Muscles Resection in Recurrent Exotropia
  7. 1187
    “…The combination of recessively inherited cone-rod dystrophy (CRD) and amelogenesis imperfecta (AI) was first reported by Jalili and Smith in 1988 in a family subsequently linked to a locus on chromosome 2q11, and it has since been reported in a second small family. …”
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    Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta
  8. 1188
    “…Extensive gingival recessions associated with cervical abrasions are common among the population. …”
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    Treatment of Gingival Recessions Associated to Cervical Abrasion Lesions with Subepithelial Connective Tissue Graft: A Case Report
  9. 1189
    “…RESULTS: The initial homozygosity screening of 13 known autosomal recessive loci resulted in negative LOD (logarithm of odds) scores. …”
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    A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family
  10. 1190
    “…More than half of all cases of retinitis pigmentosa are autosomal recessive (arRP), but the gene(s) causing arRP in most families has yet to be identified. …”
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    Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa
  11. 1191
    “…CONCLUSIONS: Deafness in ASCD is an incompletely penetrant autosomal recessive inherited disease that maps to CFA10.…”
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    Congenital Sensorineural Deafness in Australian Stumpy-Tail Cattle Dogs Is an Autosomal Recessive Trait That Maps to CFA10
  12. 1192
    “…METHODS: 272 unrelated Spanish families, 107 with autosomal recessive RP (arRP) and 165 with sporadic RP (sRP), were studied using the APEX genotyping microarray. …”
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    Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray
  13. 1193
    “…PURPOSE: Autosomal recessive bestrophinopathy (ARB) is a newly defined retinal dystrophy caused by biallelic mutations in bestrophin-1 (BEST1) and is hypothesized to represent the null bestrophin-1 phenotype in humans. …”
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    A synonymous codon variant in two patients with autosomal recessive bestrophinopathy alters in vitro splicing of BEST1
  14. 1194
    “…Our data challenge the conventional view that recessive alleles are always hypomorphic or null and that antimorphic alleles are always dominant. …”
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    Recessive Antimorphic Alleles Overcome Functionally Redundant Loci to Reveal TSO1 Function in Arabidopsis Flowers and Meristems
  15. 1195
    por Amitava, Abadan K, Darakshan, Anjum
    Publicado 2011
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    Comment on: Cut and paste: A novel method of re-attaching rectus muscles with cyanoacrylate during recessions in strabismus
  16. 1196
    “…CONCLUSION: Encephalocele within the lateral recess of the SS is a rare entity which must be suspected in patients who present with spontaneous CSF rhinorrhea. …”
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    Sternberg's canal as a cause of encephalocele within the lateral recess of the sphenoid sinus: A report of two cases
  17. 1197
    “…Retinitis pigmentosa (RP) is a highly heterogeneous genetic disease including autosomal recessive (ar), autosomal dominant (ad), and X-linked inheritance. …”
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    Two Novel Mutations in the EYS Gene Are Possible Major Causes of Autosomal Recessive Retinitis Pigmentosa in the Japanese Population
  18. 1198
    “…Here, we identified a novel homozygous p.R338* mutation in exon 4 of RP1, and speculate on the mutational mechanisms of different RP1 mutations underlying dominant and recessive RP.…”
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    Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian family
  19. 1199
    “…BACKGROUND: Hearing loss (HL) is the most frequent sensory birth defect in humans. Autosomal recessive non-syndromic HL (ARNSHL) is the most common type of hereditary HL. …”
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    Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss
  20. 1200
    “…Background: Diverse variables are implicated in the pathogenesis of gingival recession; more detailed knowledge about the relationship between the clinical presentation of gingival recession and assorted risk indicators may lead to improved patient monitoring, early intervention, and subsequent prevention. …”
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    Gingival recession and associated factors in a homogeneous Mexican adult male population: A cross-sectional study
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