Literature DB >> 1080039

[Interstitial deletion of the long arm of one 11 chromosome].

J L Taillemite, B G Morlier, C Roux.   

Abstract

A case of in testitial deletion of the long arm of chromosome 11 associated with mild facial deformity, broad skull and mental retardation is reported.

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Mesh：

Substances：

Year:  1975        PMID： 1080039

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  10 in total

1.  Partial deletion of the long arm chromosome 11 in Jacobsen syndrome.

Authors:  K S Reddy; I M Thomas; H S Narayanan
Journal:  Indian J Pediatr       Date:  1986 Jan-Feb       Impact factor: 1.967

Review 2.  Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

Authors:  E K Pivnick; G V Velagaleti; R S Wilroy; M E Smith; S R Rose; R E Tipton; A T Tharapel
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

3.  Partial deletion of the long arm of chromosome 11 the Jacobsen syndrome.

Authors:  K S Reddy; I M Thomas; H S Narayanan
Journal:  Indian J Pediatr       Date:  1984 May-Jun       Impact factor: 1.967

4.  Fragile site long arm chromosome 16.

Authors:  K Sørensen; J Nielsen; V Holm; J Haahr
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

5.  The association of a lymphoreticular malignancy with an 11q deletion: a coincidence or a cancer susceptibility?

Authors:  N L Rudd; I E Teshima
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

6.  11q aneuploidy: partial monosomy and trisomy in the children of a mother with a t(3;11)(p27;q23) translocation.

Authors:  M A Ridler; J A McKeown
Journal:  Hum Genet       Date:  1979-11-01       Impact factor: 4.132

7.  Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.

Authors:  A Schinzel; P Auf der Maur; H Moser
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

8.  Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype.

Authors:  B M Lippe; R S Sparkes; B Fass; L Neidengard
Journal:  J Med Genet       Date:  1980-12       Impact factor: 6.318

9.  Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male.

Authors:  Ioannis Papoulidis; Vassilis Paspaliaris; Elisavet Siomou; Sandro Orru; Roberta Murru; Stavros Sifakis; Petros Nikolaidis; Antonios Garas; Sotirios Sotiriou; Loretta Thomaidis; Emmanouil Manolakos
Journal:  Mol Cytogenet       Date:  2015-09-17       Impact factor: 2.009

Review 10.  Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review.

Authors:  Renata Nacinovich; Nicoletta Villa; Serena Redaelli; Fiorenza Broggi; Monica Bomba; Patrizia Stoppa; Agnese Scatigno; Angelo Selicorni; Leda Dalprà; Francesca Neri
Journal:  BMC Res Notes       Date:  2014-04-17
  10 in total

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