Literature DB >> 4232719

Pericentric inversions. Report on two malformation cases suggestive of parental inversion heterozygosity.

W Schmid.   

Abstract

Mesh：

Year:  1967        PMID： 4232719

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


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  8 in total

1.  A newborn with the cat-eye syndrome.

Authors:  J P Fryns; E Eggermont; H Veresen; H Van den Berghe
Journal:  Humangenetik       Date:  1972

2.  Coloboma and anorectal malformations: a rare association with important clinical implications.

Authors:  Giulia Brisighelli; Andrea Bischoff; Marc Levitt; Jennifer Hall; Elizabeth Monti; Alberto Peña
Journal:  Pediatr Surg Int       Date:  2013-09       Impact factor: 1.827

Review 3.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  The aetiology of the cat eye syndrome reconsidered.

Authors:  G Guanti
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

Review 5.  [Cat-eye syndrome. Clinical and cytogenetical differentialdiagnosis (author's transl)].

Authors:  J Kunze; M Tolksdorf; H R Wiedemann
Journal:  Humangenetik       Date:  1975

6.  Rieger's syndrome with pericentric inversion of chromosome 6.

Authors:  M H Heinemann; R Breg; E Cotlier
Journal:  Br J Ophthalmol       Date:  1979-01       Impact factor: 4.638

7.  A case of extra small acrocentric bisatellited chromosome in a non mongoloid child.

Authors:  M Furbetta; G Rosi; M Biagioni; P Cossu; A Cao
Journal:  Humangenetik       Date:  1975-09-20

8.  The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.

Authors:  A Schinzel; W Schmid; M Fraccaro; L Tiepolo; O Zuffardi; J M Opitz; J Lindsten; P Zetterqvist; H Enell; C Baccichetti; R Tenconi; R A Pagon
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  8 in total

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