Literature DB >> 965010

A case of trisomy for the short arm of chromosome no. 9(+9(p)).

M E Käosaar, A V Mikelsaar, T A Talvik, R V Mikelsaar.   

Abstract

A new case of "free" trisomy for the short arm of No. 9 chromosome identified by Giemsa staining and "Giemsa-11 technique" is reported.

Mesh：

Year:  1976        PMID： 965010     DOI： 10.1007/BF00284440

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  11 in total

1.  Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome no. 9.

Authors:  W Schmid; D Vischer
Journal:  Humangenetik       Date:  1969

2.  [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].

Authors:  M O Rethoré; H Hoehn; H D Rott; J Couturier; B Dutrillaux; J Lejeune
Journal:  Humangenetik       Date:  1973-04-16

3.  Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9.

Authors:  M Bobrow; K Madan; P L Pearson
Journal:  Nat New Biol       Date:  1972-07-26

4.  Preferential breakage of sensitive regions of human chromosomes.

Authors:  B R Reeves; S D Lawler
Journal:  Humangenetik       Date:  1970

5.  Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.

Authors:  P E Podruch; B Weisskopf
Journal:  J Pediatr       Date:  1974-07       Impact factor: 4.406

6.  Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18.

Authors:  A J Ebbin; M G Wilson; J W Towner; J P Slaughter
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

7.  A new case of trisomy for the short arm of No. 9 chromosome.

Authors:  C Baccichetti; R Tenconi
Journal:  J Med Genet       Date:  1973-09       Impact factor: 6.318

8.  The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man.

Authors:  M Seabright
Journal:  Chromosoma       Date:  1972       Impact factor: 4.316

9.  [Enlarged secondary constriction of chromosome C9 in mother and child].

Authors:  G Schwanitz; H D Rott; M W Köllermann
Journal:  Humangenetik       Date:  1971

10.  Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.

Authors:  H Hoehn; W Engel; H Reinwein
Journal:  Humangenetik       Date:  1971
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  4 in total

1.  De novo trisomy 9pter leads to q13.

Authors:  N B Kardon; H R Salwen; M A Krauss; J G Davis; E C Jenkins
Journal:  Hum Genet       Date:  1977-06-30       Impact factor: 4.132

2.  Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings.

Authors:  M Tolksdorf; J Kunze; G Gross-Selbeck; K Sperling; R D Wegner; V Wieczorek; M Vogel
Journal:  Eur J Pediatr       Date:  1977-08-23       Impact factor: 3.183

3.  Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.

Authors:  K R Sandig; J Mücke; H Veit
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132

4.  De novo complex intra chromosomal rearrangement after ICSI: characterisation by BACs micro array-CGH.

Authors:  Serdar Kasakyan; Laurence Lohmann; Azeddine Aboura; Mazin Quimsiyeh; Yves Menezo; Gerard Tachdjian; Moncef Benkhalifa
Journal:  Mol Cytogenet       Date:  2008-12-23       Impact factor: 2.009
  4 in total

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