Literature DB >> 4458825

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

O S Alfi, R G Sanger, A E Sweeny, G N Donnell.   

Abstract

Mesh：

Year:  1974        PMID： 4458825

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  5 in total

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

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

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.  Partial monosomy 10p syndrome.

Authors:  J M Klep-de Pater; J B Bijlsma; F M Alkema
Journal:  Eur J Pediatr       Date:  1981-10       Impact factor: 3.183

4.  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

5.  The 9p-syndrome.

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

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