Literature DB >> 78183

Monosomy-7 and the Colton blood-groups.

A De Ca Chapelle, P Vuopio, R Sanger, P Teesdale.   

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Year:  1975        PMID: 78183     DOI: 10.1016/s0140-6736(75)80042-0

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  5 in total

1.  Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34----7q22.

Authors:  F Barichard; V Joulin; I Henry; M C Garel; C Valentin; R Rosa; M Cohen-Solal; C Junien
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

2.  Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement.

Authors:  K B Nielsen; F Egede; I Mouridsen; J Mohr
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

3.  Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases.

Authors:  F Pasquali; P Bernasconi; R Casalone; M Fraccaro; C Bernasconi; M Lazzarino; E Morra; E P Alessandrino; M A Marchi; R Sanger
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  Human red cell aquaporin CHIP. I. Molecular characterization of ABH and Colton blood group antigens.

Authors:  B L Smith; G M Preston; F A Spring; D J Anstee; P Agre
Journal:  J Clin Invest       Date:  1994-09       Impact factor: 14.808

5.  Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.

Authors:  P Agre; B L Smith; R Baumgarten; G M Preston; E Pressman; P Wilson; N Illum; D J Anstee; M B Lande; M L Zeidel
Journal:  J Clin Invest       Date:  1994-09       Impact factor: 14.808

  5 in total

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