Literature DB >> 5303548

[New documents of delineation of a syndrome of the deletion of the short arm of one chromosome no 4].

R A Pfeiffer.   

Abstract

Mesh:

Year:  1968        PMID: 5303548

Source DB:  PubMed          Journal:  Z Kinderheilkd        ISSN: 0044-2917


× No keyword cloud information.
  6 in total

Review 1.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

2.  The 4p-syndrome, with a report of two new cases.

Authors:  J P Fryns; E Eggermont; H Verresen; H Van den Berghe
Journal:  Humangenetik       Date:  1973

3.  Screening for minute deletions in patients with suspected cri-du-chat syndrome and apparently normal karyotype.

Authors:  H Hoehn; W Engel
Journal:  Humangenetik       Date:  1969-10

4.  Human chromosomal deficiency: the 4p--syndrome.

Authors:  E Passarge; H C Altrogge; R A Rüdiger
Journal:  Humangenetik       Date:  1970-08-17

5.  On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Authors:  K Bender; K Burckhardt
Journal:  Humangenetik       Date:  1970

6.  Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4.

Authors:  M G Wilson; J W Towner; L D Negus
Journal:  J Med Genet       Date:  1970-06       Impact factor: 6.318

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.