Literature DB >> 6413387

Reliability of the Tønnesen technique for the identification of Hunter carriers.

L Petruschka, G Machill, M Wehnert, G Seidlitz, A Knapp.   

Abstract

The procedure for the detection of Hunter carriers suggested by Tønnesen et al. (1982) was checked in different mixtures of normal and Hunter cells as well as by examination of five obligate and five potential Hunter carriers. In the presence of fructose 1-phosphate there was a strict correlation between the proportion of mutant cells in the fibroblast culture and sulphate accumulation, both in artificial cell mixtures and in native cell cultures of Hunter carriers. In all obligate heterozygotes studied, sulphate incorporation was increased by a factor of two. The new technique seems to be suitable for carrier diagnosis. Its limitations are discussed.

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Year:  1983        PMID: 6413387     DOI: 10.1007/BF00292377

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


  15 in total

1.  Iduronate sulfatase analysis of hair roots for identification of Hunter syndrome heterozygotes.

Authors:  T Yutaka; A L Fluharty; R L Stevens; H Kihara
Journal:  Am J Hum Genet       Date:  1978-11       Impact factor: 11.025

Review 2.  X-chromosome inactivation and developmental patterns in mammals.

Authors:  M F Lyon
Journal:  Biol Rev Camb Philos Soc       Date:  1972-01

3.  Hurler and Hunter syndromes: mutual correction of the defect in cultured fibroblasts.

Authors:  J C Fratantoni; C W Hall; E F Neufeld
Journal:  Science       Date:  1968-11-01       Impact factor: 47.728

4.  The William Allan Memorial Award Lecture: Genetic nosology: three approaches.

Authors:  V A McKusick
Journal:  Am J Hum Genet       Date:  1978-03       Impact factor: 11.025

5.  Demonstration of the heterozygous state in Hunter's syndrome.

Authors:  C W Booth; H L Nadler
Journal:  Pediatrics       Date:  1974-03       Impact factor: 7.124

6.  Iduronate sulfatase activity in serum, lymphocytes, and fibroblasts--simplified diagnosis of the Hunter syndrome.

Authors:  I Liebaers; E Neufeld
Journal:  Pediatr Res       Date:  1976-08       Impact factor: 3.756

7.  Reliability of the Booth-Nadler technique for the detection of Hunter heterozygotes.

Authors:  P V Donnelly; N Di Ferrante
Journal:  Pediatrics       Date:  1975-09       Impact factor: 7.124

8.  X-linked Hunter syndrome: the heterozygous phenotype in cell culture.

Authors:  B R Migeon; J A Sprenkle; I Liebaers; J F Scott; E F Neufeld
Journal:  Am J Hum Genet       Date:  1977-09       Impact factor: 11.025

9.  Prenatal monitoring for the Hunter syndrome: the heterozygous female fetus.

Authors:  W J Kleijer; P D Moody; I Liebaers; J J van de Kamp; M F Niermeijer
Journal:  Clin Genet       Date:  1979-02       Impact factor: 4.438

10.  Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate.

Authors:  T Tønnesen; C Lykkelund; F Güttler
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

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  2 in total

1.  The use of fructose 1-phosphate to detect Hunter heterozygotes in fibroblast cultures from high-risk carriers.

Authors:  T Tønnesen
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

2.  Carrier detection of Hunter syndrome (MPS II) by biochemical and DNA techniques in families at risk.

Authors:  W Schröder; L Petruschka; M Wehnert; M Zschiesche; G Seidlitz; J J Hopwood; F H Herrmann
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

  2 in total

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