Literature DB >> 913435

New chromosomal dysmorphic syndromes. 2. Trisomy 10p.

S Stengel-Rutkowski, J D Murken, R Frankenberger, M Riechert, H Spiess, A Rodewald, J Stene.   

Abstract

This is the report of a family in which a balanced translocation in the mother t(5;10)(p15;p13) led to an unbalanced chromosomal constitution in two children. It was identified by G-banding analysis as trisomy of the distal portion of the short arm of chromosome 10 (p13 leads to pter). Comparison with 15 previous reports of trisomy 10p confirms the existence of a characteristic dysmorphic syndrome.

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Year:  1977        PMID： 913435     DOI： 10.1007/bf00442193

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


  18 in total

1.  [2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].

Authors:  S Morić-Petrović; Z Laća; A Krajgher; J Milośevic
Journal:  Ann Genet       Date:  1976-09

2.  Del (10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studies.

Authors:  U Francke; C Kernahan; C Bradshaw
Journal:  Humangenetik       Date:  1975

3.  "Cri du chat" syndrome with maternal insertional translocation.

Authors:  R Berger; G Touati; J Derre; M A Ortiz; J Martinetti
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

4.  Trisomy for the short arm of chromosome No. 10.

Authors:  T W Hustinx; B G Ter Haar; J M Scheres; F J Rutten
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

5.  Precise identification of various chromosomal abnormalities.

Authors:  K Hirschhorn; M Lucas; I Wallace
Journal:  Ann Hum Genet       Date:  1973-04       Impact factor: 1.670

6.  Observations with G bonding of human chromosomes. Reduction of dye concentration in Soerensen buffered solutions is sufficient for demonstrating G bands.

Authors:  J U Walther Walther; S Stengel-Rutkowski; J D Murken
Journal:  Humangenetik       Date:  1974

7.  The dermatoglyphic pattern of the trisomy 10p syndrome.

Authors:  A Rodewald; S Stengel-Rutkowski
Journal:  Clin Genet       Date:  1978-12       Impact factor: 4.438

8.  Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).

Authors:  J M Cantu; F Salamanca; L Buentello; A Carnevale; S Armendares
Journal:  Ann Genet       Date:  1975-03

9.  Exclusion gene mapping utilizing patients with chromosome imbalance: the HL-A system as a prototype.

Authors:  R E Magenis; K Overton; H Wyandt; T Bergstrom; F Hecht; E Lovrien
Journal:  Humangenetik       Date:  1975

10.  Partial trisomy 10p.

Authors:  K P Grosse; G Schwanitz; H Singer; V Wieczorek
Journal:  Humangenetik       Date:  1975-09-10
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  6 in total

1.  Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12).

Authors:  B Dallapiccola; L Chessa; P Vignetti; E Ferrante; E Gandini
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

2.  Partial duplication of the short arm of chromosome 10. Karyotype: 46,XX,dup(10p)(pter to p12::p12::p12 to qter).

Authors:  J P Fryns; J Deroover; J Haegeman; H Van den Berghe
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

3.  New chromosomal dysmorphic syndromes. 3. Partial trisomy 3q.

Authors:  S Stengel-Rutkowski; J D Murken; V Pilar; B Dutrillaux; A Rodewald; R Goebel; R Bassermann
Journal:  Eur J Pediatr       Date:  1979-02-08       Impact factor: 3.183

4.  Two chromosomal syndromes in the same family: monosomy and trisomy for part of the short arm of chromosome 10.

Authors:  S Slinde; I L Hansteen
Journal:  Eur J Pediatr       Date:  1982-10       Impact factor: 3.183

5.  Familial translocation t(10;21)(q22;q22).

Authors:  A Delicado; I L Pajares; P Vicente; F Hawkins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

6.  Multiple abnormalities in a child with partial duplications of 10p and 13q from a 3:1 segregation of a maternal t(10;13) translocation.

Authors:  M Y Yip; J Williams; A Goddard; P Campbell; I Lambert; R W Smithells
Journal:  J Med Genet       Date:  1990-03       Impact factor: 6.318
  6 in total

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