Literature DB >> 4135219

Frequency of deletion of short arm satellites in acrocentric chromosomes.

J Nielsen, U Friedrich, A B Hreidarsson.   

Abstract

Mesh:

Year:  1974        PMID: 4135219      PMCID: PMC1013115          DOI: 10.1136/jmg.11.2.177

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


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  12 in total

1.  Atypical acrocentric chromosomes in Negro and Caucasian Mongols.

Authors:  M N Starkman; M W Shaw
Journal:  Am J Hum Genet       Date:  1967-03       Impact factor: 11.025

2.  Group G deletion syndromes.

Authors:  R P Kelch; M Franklin; R D Schmickel
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

3.  Familial occurrence of a short arm deletion of a G-group chromosome.

Authors:  M C Yoshida; T Honda
Journal:  Jinrui Idengaku Zasshi       Date:  1969-09

4.  Exclusion of marker genes from the short arm of the human chromosome D1 by deletion mapping.

Authors:  A Brogger
Journal:  Hereditas       Date:  1969       Impact factor: 3.271

5.  [Deletion of the short arm of a 13-15 chromosome, hypertelorism and Hp0 haptoglobin phenotype in the same family].

Authors:  J de Grouchy; C Salmon; D Salmon; P Maroteaux
Journal:  Ann Genet       Date:  1966-06

6.  The G deletion syndromes.

Authors:  R J Warren; D L Rimoin
Journal:  J Pediatr       Date:  1970-10       Impact factor: 4.406

7.  Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.

Authors:  C E Parker; R Koch; J Mavalwala; A Derencsenyi; A Hatashita
Journal:  Clin Pediatr (Phila)       Date:  1969-08       Impact factor: 1.168

8.  Haptoglobin: a locus on the D1 chromosome?

Authors:  W B Bias; B R Migeon
Journal:  Am J Hum Genet       Date:  1967-05       Impact factor: 11.025

9.  Unilateral fixation of the ossicular chain associated with G-group chromosome deletion.

Authors:  G Jagiello; C Faiman
Journal:  Can Med Assoc J       Date:  1967-05-27       Impact factor: 8.262

10.  Chromosome studies in a neonatal population.

Authors:  J L Hamerton; M Ray; J Abbott; C Williamson; G C Ducasse
Journal:  Can Med Assoc J       Date:  1972-04-08       Impact factor: 8.262

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  7 in total

1.  Down's syndrome and deletion of short arms of a G chromosome.

Authors:  G H Ballantyne; M I Parslow; A M Veale; D H Pullon
Journal:  J Med Genet       Date:  1977-04       Impact factor: 6.318

2.  Partial trisomy 12q: report of a case and review.

Authors:  S H Roberts; T Mattina; K M Laurence; G Sorge; L Pavone
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

3.  Stable dicentric autosome, tdic (8:22)(p23:p13), in a mentally retarded girl.

Authors:  S H Roberts; R T Howell; K M Laurence; M E Heathcote
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

Review 4.  Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.

Authors:  D P Duckett; S H Roberts
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  13q-/r(13) mosaicism.

Authors:  N Niikawa; T Tamura; F Tomiyasu; T Kajii
Journal:  J Med Genet       Date:  1980-08       Impact factor: 6.318

6.  An r(22)(p11 leads to q13) in a moderately mentally retarded girl.

Authors:  V Aller; J A Abrisqueta; M L de Torres; M A Martín-Lucas; A Pérez-Castillo; J Del Mazo
Journal:  Hum Genet       Date:  1979-10-01       Impact factor: 4.132

7.  Recurrent increased nuchal translucency: a first trimester presentation of familial 13p satellite deletion.

Authors:  I Uzun; R Has; E Alici; M Ozdemir; C Inan; S Erzincan
Journal:  Balkan J Med Genet       Date:  2016-08-02       Impact factor: 0.519

  7 in total

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