Literature DB >> 1085605

[Partial deletion of the short arm of the chromosome 9].

F Serville, D Allain, A Broustet, C Martin, M Gachet, J P Babin, J Cenraud.   

Abstract

Monosomy 9p is reported in a boy with trigonocephaly and advanced bone age.

Entities:  

Mesh：

Year:  1976        PMID： 1085605

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  7 in total

1.  A case of 9p- syndrome.

Authors:  Y Kuroki; S Yokota; H Nakai; Y Yamamoto; I Matsui
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

Review 2.  Eleven new cases of del(9p) and features from 80 cases.

Authors:  J L Huret; C Leonard; B Forestier; M O Rethoré; J Lejeune
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

3.  Short stature and microgenitalia in the 9p-syndrome.

Authors:  H P Monaghan; N J Howard
Journal:  Ir J Med Sci       Date:  1981-12       Impact factor: 1.568

4.  Partial monosomy of the short arm of chromosome 9: a distinct clinical entity.

Authors:  J Deroover; J P Fryns; C Parloir; J Haegeman; H van den Berghe
Journal:  Hum Genet       Date:  1978-10-31       Impact factor: 4.132

5.  Deletion of the short arm of chromosome 9. A clinically recognisable entity.

Authors:  J P Fryns; J C Pedersen; H Duyck; G Fabry; H Van den Berghe
Journal:  Eur J Pediatr       Date:  1980-09       Impact factor: 3.183

6.  10p- syndrome associated with multiple chromosomal abnormalities.

Authors:  F Prieto; L Badia; J A Moreno; P Barbero; F Asensi
Journal:  Hum Genet       Date:  1978-12-18       Impact factor: 4.132

7.  The 9p-syndrome.

Authors:  S J Funderburk; R S Sparkes; I Klisak
Journal:  J Med Genet       Date:  1979-02       Impact factor: 6.318
  7 in total

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