Literature DB >> 4140909

Familial mental retardation in a family with an inherited chromosome rearrangement.

A E Chudley, F Bauder, M Ray, P J McAlpine, S D Pena, J L Hamerton.   

Abstract

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Year:  1974        PMID： 4140909      PMCID： PMC1013205          DOI： 10.1136/jmg.11.4.353

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


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  33 in total

1.  IgA and partial deletions of chromosome 18.

Authors:  J G Masterson; E M Law
Journal:  Ir J Med Sci       Date:  1969-06       Impact factor: 1.568

2.  A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.

Authors:  A Valdmanis; G Pearson; A E Siegel; R H Hoeksema; J D Mann
Journal:  Ann Genet       Date:  1967-12

3.  Immunological profile in a chromosome 18 deletion syndrome with IgA deficiency.

Authors:  S C Finley; M D Cooper; W H Finley; I A Uchida; T A Noto; R F Roddam
Journal:  J Med Genet       Date:  1969-12       Impact factor: 6.318

4.  Asymmetry of chromosome number 1 pair in three generations of a phenotypically normal family.

Authors:  K L Ying; E J Ives
Journal:  Can J Genet Cytol       Date:  1968-09

5.  Differential binding of alkylating fluorochromes in human chromosomes.

Authors:  T Caspersson; L Zech; C Johansson
Journal:  Exp Cell Res       Date:  1970-06       Impact factor: 3.905

6.  Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.

Authors:  R E Magenis; F Hecht; E W Lovrien
Journal:  Science       Date:  1970-10-02       Impact factor: 47.728

7.  Absent IgA and deletions of chromosome 18.

Authors:  J M Stewart; S Go; E Ellis; A Robinson
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

8.  IgA deficiency associated with partial deletion of chromosome 18.

Authors:  M Feingold; R S Schwartz; L Atkins; R Anderson; C S Bartsocas; D L Page; J W Littlefield
Journal:  Am J Dis Child       Date:  1969-02

9.  Probable assignment of the alpha locus of haptoglobin to chromome 16 in man.

Authors:  E B Robson; P E Polani; S J Dart; P A Jacobs; J H Renwick
Journal:  Nature       Date:  1969-09-13       Impact factor: 49.962

10.  Probable assignment of the Duffy blood group locus to chromosome 1 in man.

Authors:  R P Donahue; W B Bias; J H Renwick; V A McKusick
Journal:  Proc Natl Acad Sci U S A       Date:  1968-11       Impact factor: 11.205
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  13 in total

Review 1.  Intrachromosomal insertions: a case report and a review.

Authors:  K Madan; F H Menko
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

2.  Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.

Authors:  M Y Yip; M Selikowitz; N Don; A Kovacic; S Purvis-Smith; P R Lam-Po-Tang
Journal:  J Med Genet       Date:  1987-11       Impact factor: 6.318

3.  Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement.

Authors:  K B Nielsen; F Egede; I Mouridsen; J Mohr
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

4.  Obesity and abnormal behaviour associated with interstitial deletion of chromosome 18 (q12.2q21.1).

Authors:  G N Wilson; A A Al Saadi
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

5.  A case of inverted insertion assessed by R and G banding.

Authors:  M A de Arce; E Law; L Martin; J G Masterson
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

6.  A familial insertion involving an active nucleolar organiser within chromosome 12.

Authors:  J L Watt; D A Couzin; D J Lloyd; G S Stephen; E McKay
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

7.  Partial trisomy 18q in a newborn with typical 18 trisomy phenotype.

Authors:  J P Fryns; F Detavernier; A van Fleteren; H van den Berghe
Journal:  Hum Genet       Date:  1978-10-31       Impact factor: 4.132

8.  Segregation of an insertional chromosome rearrangement in 3 generations.

Authors:  K E Toomey; T Mohandas; R S Sparkes; M M Kaback; D L Rimoin
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

9.  The human complement after trypsin pretreatment as compared to the Paris standard.

Authors:  M Ray; N Canning; J L Hamerton
Journal:  Humangenetik       Date:  1975-08-29

10.  Trisomy 18q. A case report and review of karyotype-phenotype correlations.

Authors:  R Matsuoka; S Matsuyama; Y Yamamoto; Y Kuroki; I Matsui
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
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