Literature DB >> 3714482

An XmnI RFLP at the subtelomeric Xp locus DXS31 [HGM7, LA, 1985].

K Wrogemann, M Koenig, Y Alembik, J L Mandel.   

Abstract

Mesh：

Year:  1986        PMID： 3714482      PMCID： PMC339875          DOI： 10.1093/nar/14.10.4377

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  1 in total

1.  A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

Authors:  M Koenig; G Camerino; R Heilig; J L Mandel
Journal:  Nucleic Acids Res       Date:  1984-05-25       Impact factor: 16.971
  1 in total
  3 in total

1.  An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry.

Authors:  R E Schnur; B J Trask; G van den Engh; H H Punnett; M Kistenmacher; M A Tomeo; R E Naids; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

2.  Three cases of 45,X/46,XYnf mosaicism. Molecular analysis revealed heterogeneity of the nonfluorescent Y chromosome.

Authors:  D Gänshirt-Ahlert; I H Pawlowitzki; A Gal
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

3.  Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

Authors:  T Meitinger; B Heye; C Petit; J Levilliers; A Golla; C Moraine; B Dalla Piccola; W G Sippell; J Murken; A Ballabio
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025
  3 in total

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