Literature DB >> 7239524

4p- syndrome in a girl with translocation t(1;4)(q11;p16)mat.

C Stoll, A Pennerath, C Lausecker.   

Abstract

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Year:  1981        PMID： 7239524     DOI： 10.1007/bf00274704

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  7 in total

1.  Translocation 4p-- syndrome: a general review.

Authors:  W R Centerwall; W P Thompson; I E Allen; C D Fobes
Journal:  Am J Dis Child       Date:  1975-03

2.  4p- phenotype in an infant with t(4p-;19p or q+)mat translocation.

Authors:  R L Neu; R J Shott; L I Gardner
Journal:  Am J Dis Child       Date:  1975-03

3.  Human Q and C chromosomal variations: distribution and incidence.

Authors:  W H McKenzie; H A Lubs
Journal:  Cytogenet Cell Genet       Date:  1975

4.  Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over.

Authors:  A P Craig-Holmes; F B Moore; M W Shaw
Journal:  Am J Hum Genet       Date:  1975-03       Impact factor: 11.025

5.  Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.

Authors:  K Hirschhorn; H L Cooper; I L Firschein
Journal:  Humangenetik       Date:  1965

6.  [Deficiency on the short arms of a chromosome No. 4].

Authors:  U Wolf; H Reinwein; R Porsch; R Schröter; H Baitsch
Journal:  Humangenetik       Date:  1965

7.  Ophthalmic features of chromosome deletion 4p- (Wolf-Hirschhorn syndrome).

Authors:  L M Wilcox; L Bercovitch; R O Howard
Journal:  Am J Ophthalmol       Date:  1978-12       Impact factor: 5.258
  7 in total
  1 in total

1.  Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].

Authors:  M G Wilson; J W Towner; G S Coffin; A J Ebbin; E Siris; P Brager
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  1 in total

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