Literature DB >> 6431894

[The r(14) syndrome. 3 new observations].

S Gilgenkrantz, A Morali, M Vidailhet, R Saura, F Serville, D Fontan, C Moraine.   

Abstract

Three observations of r(14) are reported. Constant features of r(14) syndrome are the following: moderate but typical craniofacial dysmorphism, seizures and other neurological abnormalities, abnormal retinal pigmentation, and recurrent respiratory infections. The value of gene dosage evaluation for genes mapped to the distal segment of 14q, particularly the Ig heavy chain genes, is emphasized.

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Year:  1984        PMID: 6431894

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


  5 in total

1.  Distal trisomy 14q. II. Molecular study of the 14q32 locus in two cases of chromosome 14 rearrangements with partial duplication.

Authors:  G Keyeux; S Gilgenkrantz; G Lefranc; M P Lefranc
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

Review 2.  Terminal deletion (14)(q32.3): a new case.

Authors:  N Telford; D A Thomson; M J Griffiths; S Ilett; J L Watt
Journal:  J Med Genet       Date:  1990-04       Impact factor: 6.318

3.  Molecular characterization of a ring chromosome 14 showing that the PI locus is centromeric to the D14S1 and IGH loci.

Authors:  G Keyeux; S Gilgenkrantz; G Lefranc; M P Lefranc
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

4.  Retinal/macular pigmentation in conjunction with ring 14 chromosome.

Authors:  P J Howard; D Clark; J Dearlove
Journal:  Hum Genet       Date:  1988-10       Impact factor: 4.132

5.  A Case of Autism with Ring Chromosome 14.

Authors:  Massoumeh Tajeran; Fatemeh Baghbani; Mohammad Hassanzadeh-Nazarabadi
Journal:  Iran J Public Health       Date:  2013-11       Impact factor: 1.429

  5 in total

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