Literature DB >> 5159532

An inherited X-autosome translocation in man.

K E Buckton, P A Jacobs, L A Rae, M S Newton, R Sanger.   

Abstract

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Year:  1971        PMID: 5159532     DOI: 10.1111/j.1469-1809.1956.tb01390.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


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  34 in total

1.  Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21).

Authors:  J Couturier; B Dutrillaux; P Garber; O Raoul; M F Croquette; J C Fourlinnie; E Maillard
Journal:  Hum Genet       Date:  1979-07-18       Impact factor: 4.132

Review 2.  The critical region on the human Xq.

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

6.  Short-arm deletion of an X chromosome (45,XO/46,XX p--).

Authors:  P Kaiser; K Gerhard-Ratschow; B Zabel; E Daume
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

7.  Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriers.

Authors:  C Turleau; F Chavin-Colin; J de Grouchy; G Repessé; P Beauvais
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

8.  Women heterozygous for deficiency of the (p21 leads to pter) region of the X chromosome are fertile.

Authors:  M Fraccaro; P Maraschio; F Pasquali; S Scappaticci
Journal:  Hum Genet       Date:  1977-12-23       Impact factor: 4.132

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

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

10.  Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly.

Authors:  M J Faed; M A Lamont; K Baxby
Journal:  J Med Genet       Date:  1982-02       Impact factor: 6.318

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