Literature DB >> 8673111

A paternal wash in Apert syndrome.

C Sapienza.   

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Year:  1996        PMID: 8673111     DOI: 10.1038/ng0596-9

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


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  5 in total

Review 1.  Paternal factors and schizophrenia risk: de novo mutations and imprinting.

Authors:  D Malaspina
Journal:  Schizophr Bull       Date:  2001       Impact factor: 9.306

2.  Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).

Authors:  A Carrié; F Piccolo; F Leturcq; C de Toma; K Azibi; C Beldjord; J M Vallat; L Merlini; T Voit; C Sewry; J A Urtizberea; N Romero; F M Tomé; M Fardeau; Y Sunada; K P Campbell; J C Kaplan; M Jeanpierre
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

Review 3.  The high spontaneous mutation rate: is it a health risk?

Authors:  J F Crow
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-05       Impact factor: 11.205

4.  An aetiological classification of birth defects for epidemiological research.

Authors:  D Wellesley; P Boyd; H Dolk; S Pattenden
Journal:  J Med Genet       Date:  2005-01       Impact factor: 6.318

5.  Methylation levels at selected CpG sites in the factor VIII and FGFR3 genes, in mature female and male germ cells: implications for male-driven evolution.

Authors:  O El-Maarri; A Olek; B Balaban; M Montag; H van der Ven; B Urman; K Olek; S H Caglayan; J Walter; J Oldenburg
Journal:  Am J Hum Genet       Date:  1998-10       Impact factor: 11.025

  5 in total

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