Literature DB >> 7338444

Short stature and microgenitalia in the 9p-syndrome.

H P Monaghan, N J Howard.   

Abstract

Mesh：

Year:  1981        PMID： 7338444     DOI： 10.1007/bf02938279

Source DB:  PubMed          Journal:  Ir J Med Sci        ISSN： 0021-1265            Impact factor:   1.568


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  8 in total

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

Authors:  F Serville; D Allain; A Broustet; C Martin; M Gachet; J P Babin; J Cenraud
Journal:  Ann Genet       Date:  1976-06

2.  The 9p- syndrome.

Authors:  O S Alfi; G N Donnell; P W Allderdice; A Derencsenyi
Journal:  Ann Genet       Date:  1976-03

3.  The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocation.

Authors:  E Orye; H Verhaaren; A M Van den Bogaert-Van Heesvelde
Journal:  Clin Genet       Date:  1975-11       Impact factor: 4.438

4.  The deletion 9p syndrome. A 61-year-old man with deletion of short arm 9.

Authors:  J Nielsen; A Homma; F Christiansen; K Rasmussen; P Saldaña-Garcia
Journal:  Clin Genet       Date:  1977-08       Impact factor: 4.438

5.  Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.

Authors:  O Alfi; G N Donnell; B F Crandall; A Derencsenyi; R Menon
Journal:  Ann Genet       Date:  1973-03

6.  46, Del (9) (22:), a new deletion syndrome.

Authors:  O S Alfi; R G Sanger; A E Sweeny; G N Donnell
Journal:  Birth Defects Orig Artic Ser       Date:  1974

7.  C-group chromosome abnormality (? 10p-). Occurrence in a child with multiple malformations.

Authors:  D Elliott; G H Thomas; C J Condron; N Khuri; F Richardson
Journal:  Am J Dis Child       Date:  1970-01

8.  The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunction.

Authors:  F Bergamo; F Crosato; D Francesconi; F Pasqual; O Zuffardi
Journal:  Clin Genet       Date:  1977-03       Impact factor: 4.438
  8 in total
  2 in total

Review 1.  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

2.  A Case Report of 9p Deletion Syndrome Associated with Partial Trisomy of 1q42.

Authors:  Ali Vahabi; Filiz Hazan; Isa Abdi Rad
Journal:  Maedica (Bucur)       Date:  2017-01
  2 in total

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