Literature DB >> 5306363

[Study of a probable linkage between a genodermatosis with an autosomal dominant transmission and the MNSs blood group system].

M Deminatti, Y Delmas-Marsalet, M Mennecier, S Marquet, P Agache, C Huriez.   

Abstract

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Year:  1968        PMID: 5306363

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


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  6 in total

Review 1.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

2.  The Dombrock system: linkage relations with other blood group loci.

Authors:  P Tippett; J Gavin; R Sanger
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

3.  Genetic mapping: chromosomes 2-5.

Authors:  B Keats
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  A Rare Syndrome Resembling Scleroderma: Huriez Syndrome.

Authors:  Nil Su Çelik; Şirin Yaşar; Sema Aytekin; Pembegül Güneş
Journal:  Skin Appendage Disord       Date:  2017-08-12

5.  Chromosome assignments of genes in man using mouse-human somatic cell hybrids: Cytoplasmic isocitrate dehydrogenase (IDH 1) and malate dehydrogenase (MDH 1) to chromosomes 2.

Authors:  R P Creagan; B Carritt; S Chen; R Kucherlapati; F A McMorris; F Ricciuti; Y H Tan; J A Tischfield; F H Ruddle
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

6.  Poikiloderma a varied presentation - Huriez syndrome.

Authors:  Priyadarshini Kharge; Carol Fernendes; Vijayeeta Jairath; Madan Mohan; Suresh Chandra
Journal:  Indian Dermatol Online J       Date:  2015 Jan-Feb
  6 in total

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