Literature DB >> 14564160

Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literature.

Anne M Slavotinek, Felicitas Lacbawan.   

Abstract

We report a 16 year old African American female with an interstitial deletion of chromosome 13 comprising approximately 40% of the long arm of this chromosome [karyotype 46,XX, del(13)(q14.12q31.2)]. We believe that this case is interesting because of the large size of the chromosome deletion, the severe growth retardation seen in the proband and her prolonged survival.

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Year:  2003        PMID: 14564160     DOI: 10.1097/01.mcd.0000072160.33788.1f

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  4 in total

1.  Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.

Authors:  William B Dobyns; Ghayda Mirzaa; Susan L Christian; Kristin Petras; Jessica Roseberry; Gary D Clark; Cynthia J R Curry; Donna McDonald-McGinn; Livija Medne; Elaine Zackai; Julie Parsons; Dina J Zand; Fuki M Hisama; Christopher A Walsh; Richard J Leventer; Christa L Martin; Marzena Gajecka; Lisa G Shaffer
Journal:  Am J Med Genet A       Date:  2008-07-01       Impact factor: 2.802

2.  Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions.

Authors:  Diana Mitter; Reinhard Ullmann; Artur Muradyan; Ludger Klein-Hitpass; Deniz Kanber; Katrin Ounap; Marc Kaulisch; Dietmar Lohmann
Journal:  Eur J Hum Genet       Date:  2011-04-20       Impact factor: 4.246

3.  13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome - case report and review of the literature.

Authors:  Ilaria Bestetti; Alessandra Sironi; Ilaria Catusi; Milena Mariani; Daniela Giardino; Siranoush Manoukian; Donatella Milani; Lidia Larizza; Chiara Castronovo; Palma Finelli
Journal:  Mol Cytogenet       Date:  2018-09-19       Impact factor: 2.009

4.  13q Deletion Syndrome Involving RB1: Characterization of a New Minimal Critical Region for Psychomotor Delay.

Authors:  Flavia Privitera; Arianna Calonaci; Gabriella Doddato; Filomena Tiziana Papa; Margherita Baldassarri; Anna Maria Pinto; Francesca Mari; Ilaria Longo; Mauro Caini; Daniela Galimberti; Theodora Hadjistilianou; Sonia De Francesco; Alessandra Renieri; Francesca Ariani
Journal:  Genes (Basel)       Date:  2021-08-26       Impact factor: 4.096

  4 in total

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