Literature DB >> 914285

A casuistic report on the Gruber or Meckel syndrome.

P Altmann, P Wagenbichler, A Schaller.   

Abstract

A case of Meckel or Gruber syndrome is reported, together with a survey of the relevant literature of recent years (1971-1977), in reference to a probably autosomal recessive inheritance of this malformation.

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Year:  1977        PMID： 914285     DOI： 10.1007/bf00402165

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


  5 in total

1.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

2.  Analysis of the human karyotype by the recent banding techniques.

Authors:  W Schnedl
Journal:  Arch Genet (Zur)       Date:  1973

3.  The Meckel syndrome with limited expression in relatives.

Authors:  N Fitch; L Pinsky
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

4.  Encephalocele, polycystic kidneys, and polydactyly as an autosomal recessive trait simulating certain other disorders: the Meckel syndrome.

Authors:  S Mecke; E Passarge
Journal:  Ann Genet       Date:  1971-06

5.  Genetics of the Meckel syndrome (dysencephalia splanchnocystica).

Authors:  Y E Hsia; M Bratu; A Herbordt
Journal:  Pediatrics       Date:  1971-08       Impact factor: 7.124
  5 in total
  3 in total

1.  The Meckel Syndrome. Pathological and cytogenetic observations in eight cases.

Authors:  P Moerman; E Verbeken; J P Fryns; P Goddeeris; J M Lauweryns
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

2.  Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome?

Authors:  F Majewski; H Stöss; T Goecke; H Kemperdick
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

Review 3.  Genetics of microphthalmos.

Authors:  M Warburg
Journal:  Int Ophthalmol       Date:  1981-08       Impact factor: 2.031
  3 in total

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