Literature DB >> 1675683

A cytogenetic and molecular study of a series of 45,X fetuses and their parents.

A Cockwell1, M MacKenzie, S Youings, P Jacobs.   

Abstract

The parental origin of the single X chromosome in 10 45,X fetuses was studied using DNA restriction fragment length polymorphisms. In six the single X was maternal in origin, in one it was paternal, and in one the results were consistent with a paternal origin. Therefore the parental origin of the X in 45,X fetuses that survive to the second or third trimester of pregnancy is similar to that of spontaneous abortions and live births with a 45,X constitution. The mothers of two of the fetuses were themselves found to have an abnormal sex chromosome complement, but in neither case did it appear to be related to the chromosome abnormality in the fetus.

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Year:  1991        PMID: 1675683      PMCID: PMC1016795          DOI: 10.1136/jmg.28.3.151

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  14 in total

1.  Xg groups and sex chromosome abnormalities in people of northern European ancestry: an addendum.

Authors:  R Sanger; P Tippett; J Gavin; P Teesdale; G L Daniels
Journal:  J Med Genet       Date:  1977-06       Impact factor: 6.318

2.  A simple salting out procedure for extracting DNA from human nucleated cells.

Authors:  S A Miller; D D Dykes; H F Polesky
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

3.  The parental origin of the extra X chromosome in 47,XXX females.

Authors:  K M May; P A Jacobs; M Lee; S Ratcliffe; A Robinson; J Nielsen; T J Hassold
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

4.  Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome.

Authors:  C M Krauss; R N Turksoy; L Atkins; C McLaughlin; L G Brown; D C Page
Journal:  N Engl J Med       Date:  1987-07-16       Impact factor: 91.245

5.  The incidence of sex-chromosome anomalies following irradiation of mouse spermatogonia with single or fractionated doses of x-rays.

Authors:  L B Russell; C S Montgomery
Journal:  Mutat Res       Date:  1974-12       Impact factor: 2.433

6.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365

7.  Chromosomal abnormalities in human sperm: comparisons among four healthy men.

Authors:  B Brandriff; L Gordon; L Ashworth; G Watchmaker; A Carrano; A Wyrobek
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  X-autosome translocations: cytogenetic characteristics and their consequences.

Authors:  M G Mattei; J F Mattei; S Ayme; F Giraud
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

9.  Fertility in 47,XXX and 45,X patients.

Authors:  J Dewhurst
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318

10.  The chromosome constitution of 1000 human spermatozoa.

Authors:  R H Martin; W Balkan; K Burns; A W Rademaker; C C Lin; N L Rudd
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

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  19 in total

1.  Molecular studies of parental origin and mosaicism in 45,X conceptuses.

Authors:  T Hassold; D Pettay; A Robinson; I Uchida
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

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Review 3.  Sexual differentiation of brain and other tissues: Five questions for the next 50 years.

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4.  FISH with whole chromosome and telomeric probes demonstrates huge karyotypic reorganization with ITS between two species of Oryzomyini (Sigmodontinae, Rodentia): Hylaeamys megacephalus probes on Cerradomys langguthi karyotype.

Authors:  Cleusa Yoshiko Nagamachi; Julio Cesar Pieczarka; Patricia Caroline Mary O'Brien; Jamilly Amaral Pinto; Stella Miranda Malcher; Adenilson Leão Pereira; Jorge das Dores Rissino; Ana Cristina Mendes-Oliveira; Rogério Vieira Rossi; Malcolm Andrew Ferguson-Smith
Journal:  Chromosome Res       Date:  2013-03-14       Impact factor: 5.239

5.  Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci.

Authors:  Bernhard Zimmermann; Matthew Hill; George Gemelos; Zachary Demko; Milena Banjevic; Johan Baner; Allison Ryan; Styrmir Sigurjonsson; Nikhil Chopra; Michael Dodd; Brynn Levy; Matthew Rabinowitz
Journal:  Prenat Diagn       Date:  2012-10-30       Impact factor: 3.050

Review 6.  Value of growth hormone treatment in Turner's syndrome.

Authors:  P Saenger
Journal:  Endocrine       Date:  2000-04       Impact factor: 3.925

7.  DNMT3L is a regulator of X chromosome compaction and post-meiotic gene transcription.

Authors:  Natasha M Zamudio; Hamish S Scott; Katja Wolski; Chi-Yi Lo; Charity Law; Dillon Leong; Sarah A Kinkel; Suyinn Chong; Damien Jolley; Gordon K Smyth; David de Kretser; Emma Whitelaw; Moira K O'Bryan
Journal:  PLoS One       Date:  2011-03-31       Impact factor: 3.240

8.  Functional and regulatory aspects of oxidative stress response in X monosomy.

Authors:  Vinayak S Biradar; Shriram N Rajpathak; Suraj R Joshi; Deepti D Deobagkar
Journal:  In Vitro Cell Dev Biol Anim       Date:  2021-09-09       Impact factor: 2.416

9.  Studying early lethality of 45,XO (Turner's syndrome) embryos using human embryonic stem cells.

Authors:  Achia Urbach; Nissim Benvenisty
Journal:  PLoS One       Date:  2009-01-12       Impact factor: 3.240

10.  Hemodynamic Abnormalities in the Aorta of Turner Syndrome Girls.

Authors:  Lauren Johnston; Ruth Allen; Pauline Hall Barrientos; Avril Mason; Asimina Kazakidi
Journal:  Front Cardiovasc Med       Date:  2021-06-01
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