Literature DB >> 8054971

Chromosome 4p16 and osteochondroplasias.

M Urioste, M L Martinez-Frias, E Bermejo, A Villa, N Jimenez, D Romero, C Nieto.   

Abstract

Mesh：

Year:  1994        PMID： 8054971     DOI： 10.1038/ng0494-334

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  2 in total

1.  Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes.

Authors:  L I al-Gazali; L Sztriha; A Dawodu; E Varady; M Bakir; A Khdir; J Johansen
Journal:  J Med Genet       Date:  1999-06       Impact factor: 6.318

2.  Achondroplasia is defined by recurrent G380R mutations of FGFR3.

Authors:  G A Bellus; T W Hefferon; R I Ortiz de Luna; J T Hecht; W A Horton; M Machado; I Kaitila; I McIntosh; C A Francomano
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025
  2 in total

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