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  1. 581
    “…Over 1200 recessive disease genes have been described in humans. …”
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    Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles
  2. 582
    “…Clinical parameters such as recession depth, recession width, surface area, width of keratinized gingival (KG), clinical attachment level (CAL), probing depth, plaque index and gingival index were evaluated at 3, 6 and 9 months post-surgery. …”
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    Use of autologous platelet rich plasma to treat gingival recession in esthetic periodontal surgery
  3. 583
    por Jaureguiberry, Graciana, De la Dure-Molla, Muriel, Parry, David, Quentric, Mickael, Himmerkus, Nina, Koike, Toshiyasu, Poulter, James, Klootwijk, Enriko, Robinette, Steven L., Howie, Alexander J., Patel, Vaksha, Figueres, Marie-Lucile, Stanescu, Horia C., Issler, Naomi, Nicholson, Jeremy K., Bockenhauer, Detlef, Laing, Christopher, Walsh, Stephen B., McCredie, David A., Povey, Sue, Asselin, Audrey, Picard, Arnaud, Coulomb, Aurore, Medlar, Alan J., Bailleul-Forestier, Isabelle, Verloes, Alain, Le Caignec, Cedric, Roussey, Gwenaelle, Guiol, Julien, Isidor, Bertrand, Logan, Clare, Shore, Roger, Johnson, Colin, Inglehearn, Christopher, Al-Bahlani, Suhaila, Schmittbuhl, Matthieu, Clauss, François, Huckert, Mathilde, Laugel, Virginie, Ginglinger, Emmanuelle, Pajarola, Sandra, Spartà, Giuseppina, Bartholdi, Deborah, Rauch, Anita, Addor, Marie-Claude, Yamaguti, Paulo M., Safatle, Heloisa P., Acevedo, Ana Carolina, Martelli-Júnior, Hercílio, dos Santos Netos, Pedro E., Coletta, Ricardo D., Gruessel, Sandra, Sandmann, Carolin, Ruehmann, Denise, Langman, Craig B., Scheinman, Steven J., Ozdemir-Ozenen, Didem, Hart, Thomas C., Hart, P. Suzanne, Neugebauer, Ute, Schlatter, Eberhard, Houillier, Pascal, Gahl, William A., Vikkula, Miikka, Bloch-Zupan, Agnès, Bleich, Markus, Kitagawa, Hiroshi, Unwin, Robert J., Mighell, Alan, Berdal, Ariane, Kleta, Robert
    Publicado 2013
    “…CONCLUSIONS: This au-tosomal recessive disorder, also known as enamel renal syndrome, of FAM20A causes nephrocalcinosis and amelogenesis imperfecta. …”
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    Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations
  4. 584
    “…CONCLUSIONS: Here, we report a truncating mutation in the MEOX1 gene in a KFS family with an autosomal recessive trait. Together with another recently reported study and the knockout mouse model, our results suggest that mutations in MEOX1 cause a recessive KFS phenotype in humans.…”
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    Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype
  5. 585
    “…This is the first report linking CREB3L1 to human recessive OI, thereby expanding the OI gene spectrum.…”
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    Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans
  6. 586
    “…To remedy this problem, we developed a short pre-/post-test, an in-class activity for small groups, and a series of clicker questions about recessive epistasis in the context of a signaling pathway that intersects with an enzymatic pathway. …”
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    What’s Downstream? A Set of Classroom Exercises to Help Students Understand Recessive Epistasis
  7. 587
    “…Objective(s): To determine the fetal discernment in suspected cases of sex linked recessive disease in the first trimester of pregnancy. …”
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    Prenatal sex determination in suspicious cases of X-linked recessive diseases by the amelogenin gene
  8. 588
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    Oral Manifestation of Autosomal Recessive Congenital Ichthyosis in a 2-Year-Old Patient
  9. 589
    “…BACKGROUND: Many children, in particular girls, do not reach the recommended amount of daily physical activity. School recess provides an opportunity for both boys and girls to be physically active, but barriers to recess physical activity are not well understood. …”
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    Barriers for recess physical activity: a gender specific qualitative focus group exploration
  10. 590
    por Nwhator, SO
    Publicado 2014
    “…Gingival recession is commonly associated with plaque-induced inflammation and calculus. …”
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    Gingival Recession in a Child-Patient; Easily Missed Etiologies: Case Report with Video
  11. 591
    “…Most patients show autosomal recessive patterns of inheritance. CASE PRESENTATION: We report a case of two sisters with clinically epidermodysplasia verruciformis specific lesions on the face, neck, trunk, and extremities. …”
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    Two sisters reveal autosomal recessive inheritance of epidermodysplasia verruciformis: a case report
  12. 592
    “…Structure-function implication on a novel homozygous Trp250/Gly mutation of transglutaminase-1 (TGM1) observed in a patient of autosomal recessive congenital ichthyosis is invoked from a bioinformatics analysis. …”
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    A Novel Mutation in the Transglutaminase-1 Gene in an Autosomal Recessive Congenital Ichthyosis Patient
  13. 593
    “…BACKGROUND: A subset of hereditary cerebellar ataxias is inherited as autosomal recessive traits (ARCAs). Classification of recessive ataxias due to phenotypic differences in the cerebellum and cerebellar structures is constantly evolving due to new identified disease genes. …”
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    STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
  14. 594
    “…Autosomal recessive hypotrichosis simplex with woolly hair is a rare dermatological disorder, characterized by sparse hair and tightly curled hair. …”
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    Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
  15. 595
    “…Lateral sliding flaps have been used for localized recession, but they are rarely used for multiple recessions. …”
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    Multiple Marginal Tissue Recession Treated with a Simplified Lateral Sliding Flap Technique
  16. 596
    “…OBJECTIVE(S): Genetic analysis of two consanguineous Pakistani families with localized autosomal recessive hypotrichosis was performed with the goal to establish genotype-phenotype correlation. …”
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    Genetic dissection of two Pakistani families with consanguineous localized autosomal recessive hypotrichosis (LAH)
  17. 597
    por Chun, Bo Young, Kang, Kyung Min
    Publicado 2015
    “…The aim of this study was to evaluate the efficacy of slanted recession of the lateral rectus muscle for intermittent exotropia with convergence insufficiency. …”
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    Early Results of Slanted Recession of the Lateral Rectus Muscle for Intermittent Exotropia with Convergence Insufficiency
  18. 598
    “…BACKGROUND: Physical activity patterns during recess have been poorly described among adolescents. …”
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    Physical activity during recess among 13–14 year old Mexican girls
  19. 599
    “…INTRODUCTION: The use of hematopoietic cell transplantation (HCT) has previously been shown to ameliorate cutaneous blistering in pediatric patients with recessive dystrophic epidermolysis bullosa (RDEB), an inherited skin disorder that results from loss-of-function mutations in COL7A1 and manifests as deficient or absent type VII collagen protein (C7) within the epidermal basement membrane. …”
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    Preconditioning of mesenchymal stem cells for improved transplantation efficacy in recessive dystrophic epidermolysis bullosa
  20. 600
    “…We report a naturally-occurring, stationary, autosomal recessive phenotype in beagle dogs with normal daylight vision but absent night vision. …”
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    A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness
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