Literature DB >> 4704858

X inactivation in man: a woman with t(Xq--;12q+).

G E Sarto, E Therman, K Patau.   

Abstract

Entities:  

Mesh:

Year:  1973        PMID: 4704858      PMCID: PMC1762535     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  14 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.  Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

Authors:  T H Thelen; D J Abrams; R O Fisch
Journal:  Am J Hum Genet       Date:  1971-07       Impact factor: 11.025

3.  [Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+].

Authors:  W Engel; W Vogel; H Reinwein
Journal:  Cytogenetics       Date:  1971

4.  Evidence for X-X chromosome translocation in humans.

Authors:  A K Sinha; J J Nora
Journal:  Ann Hum Genet       Date:  1969-10       Impact factor: 1.670

5.  Presumptive x-autosome translocation in a cow: preferential inactivation of the normal x chromosome.

Authors:  I Gustavsson; M Fraccaro; L Tiepolo; J Lindsten
Journal:  Nature       Date:  1968-04-13       Impact factor: 49.962

6.  Fluorescent labeling of chromosomal DNA: superiority of quinacrine mustard to quinacrine.

Authors:  T Caspersson; L Zech; E J Modest
Journal:  Science       Date:  1970-11-13       Impact factor: 47.728

7.  Comparative studies on X-autosome translocations in the mouse. II. Inactivation of autosomal loci, segregation, and mapping of autosomal breakpoints in five T (X;1) S.

Authors:  L B Russell; C S Montgomery
Journal:  Genetics       Date:  1970-02       Impact factor: 4.562

8.  Possible X-autosomal translocation in a girl with gonadal dysgenesis.

Authors:  M J Thorburn; P A Martin; U N Pathak
Journal:  J Med Genet       Date:  1970-12       Impact factor: 6.318

9.  Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis.

Authors:  M M Cohen; V J Capraro; N Takagi
Journal:  Ann Hum Genet       Date:  1967-05       Impact factor: 1.670

10.  Chromosomal abnormalities in the human population: estimation of rates based on New Haven newborn study.

Authors:  H A Lubs; F H Ruddle
Journal:  Science       Date:  1970-07-31       Impact factor: 47.728

View more
  42 in total

Review 1.  The critical region on the human Xq.

Authors:  E Therman; R Laxova; B Susman
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

Review 2.  Intrachromosomal insertions: a case report and a review.

Authors:  K Madan; F H Menko
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

3.  Aspermia, associated with a presumably balanced X/autosomal translocation karyotype 46, Y, t (X;5) (q28;q11).

Authors:  S Stengel-Rutkowski; H Zankl; A Rodewald; S Scharrer; J P Chaudhuri; K D Zang
Journal:  Hum Genet       Date:  1976-01-28       Impact factor: 4.132

4.  Short stature in a girl with a terminal Xp deletion distal to DXYS15: localisation of a growth gene(s) in the pseudoautosomal region.

Authors:  T Ogata; P Goodfellow; C Petit; M Aya; N Matsuo
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

5.  A familial X;autosome translocation associated with Becker type muscular dystrophy?

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

6.  BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes.

Authors:  S A Latt; H F Willard; P S Gerald
Journal:  Chromosoma       Date:  1976-08-17       Impact factor: 4.316

7.  Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure.

Authors:  Artur Beke; Henriett Piko; Iren Haltrich; Judit Csomor; Andras Matolcsy; György Fekete; Janos Rigo; Veronika Karcagi
Journal:  Mol Cytogenet       Date:  2013-12-20       Impact factor: 2.009

8.  Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error.

Authors:  S Schwartz; M F Schwartz; S R Panny; C J Peterson; E Waters; M M Cohen
Journal:  Am J Hum Genet       Date:  1986-05       Impact factor: 11.025

9.  Structural aberration of the X chromosome in a patient with gonadal dysgenesis: an approach to karyotype-phenotype correlation.

Authors:  M Varella-Garcia; E H Tajara; A R Gagliardi
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

10.  [Four new cases of X-autosome translocation in man (author's transl)].

Authors:  C Laurent; M C Biemont; B Dutrillaux
Journal:  Humangenetik       Date:  1975
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.