Literature DB >> 3367353

Clinical consequences of deletion 1p35.

S L Wenger1, M W Steele, D J Becker.   

Abstract

Few cases of deletion 1p have been reported. We report a case of terminal deletion 1p35 in a patient with psychological and neurological dysfunction.

Entities:  

Mesh：

Year:  1988        PMID： 3367353      PMCID： PMC1015511          DOI： 10.1136/jmg.25.4.263

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  7 in total

1.  RING-1 CHROMOSOME AND MICROCEPHALIC DWARFISM.

Authors:  R R GORDON; P COOKE
Journal:  Lancet       Date:  1964-12-05       Impact factor: 79.321

2.  Ring-1 chromosome, microcephalic dwarfism, and acute myeloid leukemia.

Authors:  M Bobrow; P M Emerson; A I Spriggs; H L Ellis
Journal:  Am J Dis Child       Date:  1973-08

3.  Monosomy 1pter.

Authors:  E Yunis; L Quintero; M Leibovici
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  The ascertainment and implications of an unbalanced translocation in the neonate. Familial 1:15 translocation.

Authors:  D Hain; M Leversha; N Campbell; A Daniel; P A Barr; J G Rogers
Journal:  Aust Paediatr J       Date:  1980-09

5.  Ring 1 chromosome and dwarfism--a possible syndrome.

Authors:  C B Wolf; J A Peterson; G A LoGrippo; L Weiss
Journal:  J Pediatr       Date:  1967-11       Impact factor: 4.406

6.  Apparently non-deleted ring-1 chromosome and extreme growth failure in a mentally retarded girl.

Authors:  B Kjessler; K H Gustavson; A Wigertz
Journal:  Clin Genet       Date:  1978-07       Impact factor: 4.438

7.  The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1.

Authors:  M W Steele; S L Wenger; L O Geweke; W L Golden
Journal:  Clin Genet       Date:  1984-01       Impact factor: 4.438
  7 in total
  5 in total

1.  De novo interstitial deletion of 1p (pter----p34.1::p32.3----qter).

Authors:  M Yoshino; Y Watanabe; N Harada; K Abe
Journal:  J Med Genet       Date:  1991-08       Impact factor: 6.318

Review 2.  Chromosomal disorders and autism.

Authors:  C Gillberg
Journal:  J Autism Dev Disord       Date:  1998-10

3.  Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

Authors:  S K Shapira; C McCaskill; H Northrup; A S Spikes; F F Elder; V R Sutton; J R Korenberg; F Greenberg; L G Shaffer
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

Review 4.  Monosomy 1p36.

Authors:  A Slavotinek; L G Shaffer; S K Shapira
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

5.  Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres.

Authors:  A Slavotinek; M Rosenberg; S Knight; L Gaunt; W Fergusson; C Killoran; J Clayton-Smith; H Kingston; R H Campbell; J Flint; D Donnai; L Biesecker
Journal:  J Med Genet       Date:  1999-05       Impact factor: 6.318
  5 in total

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