Literature DB >> 5449950

Human chromosomal deficiency: the 4p--syndrome.

E Passarge, H C Altrogge, R A Rüdiger.   

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Year:  1970        PMID： 5449950     DOI： 10.1007/bf00297640

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  20 in total

1.  Chromosome aberrations in 2159 consecutive newborn babies.

Authors:  F Sergovich; G H Valentine; A T Chen; R A Kinch; M S Smout
Journal:  N Engl J Med       Date:  1969-04-17       Impact factor: 91.245

2.  Deleted late-replicating chromosomes.

Authors:  O J Miller; W R Breg; D Warburton; D A Miller; A DeCapoa; A M Chutorian
Journal:  Lancet       Date:  1966-07-09       Impact factor: 79.321

Review 3.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

Review 4.  [On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations].

Authors:  K Bender; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1967

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

Authors:  R A Pfeiffer
Journal:  Z Kinderheilkd       Date:  1968

6.  Multiple congenital anomalies associated with a ring-D chromosome.

Authors:  R C Juberg; M S Adams; W J Venema; M G Hart
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

7.  Clusterine in deleted short-arm length among 25 cases with a Bp-chromosome.

Authors:  D A Miller; D Warburton; O J Miller
Journal:  Cytogenetics       Date:  1969

8.  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

9.  [On a case of "crying cat" syndrome with peculiar phenotypic anomalies].

Authors:  P L Giorgi; M Ceccarelli; A Paci
Journal:  Minerva Pediatr       Date:  1965-12-15       Impact factor: 1.312

10.  Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.

Authors:  A De Capoa; D Warburton; W R Breg; D A Miller; O J Miller
Journal:  Am J Hum Genet       Date:  1967-07       Impact factor: 11.025
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  5 in total

1.  Derivative chromosomal structures from a ring chromsome 4.

Authors:  R Niss; E Passarge
Journal:  Humangenetik       Date:  1975-05-26

Review 2.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

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

3.  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

4.  Further observations on a previously reported case of 4p--syndrome.

Authors:  I Subrt; B Blehová
Journal:  Humangenetik       Date:  1972

5.  An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality.

Authors:  N L Shannon; E L Maltby; A S Rigby; O W Quarrell
Journal:  J Med Genet       Date:  2001-10       Impact factor: 6.318
  5 in total

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