Literature DB >> 7311257

On the heritability of rickets, a common disease (Mendel, mammals and phosphate).

C R Scriver, H S Tenenhouse.   

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Year:  1981        PMID: 7311257

Source DB:  PubMed          Journal:  Johns Hopkins Med J        ISSN: 0021-7263


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  7 in total

1.  2001 ASHG Award for Excellence in Education. ... And know the place for the first time.

Authors:  Charles R Scriver
Journal:  Am J Hum Genet       Date:  2002-01-04       Impact factor: 11.025

2.  The Gy mutation: another cause of X-linked hypophosphatemia in mouse.

Authors:  M F Lyon; C R Scriver; L R Baker; H S Tenenhouse; J Kronick; S Mandla
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

Review 3.  Vitamins: an evolutionary perspective.

Authors:  C R Scriver
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

4.  Genetic screening: implications for preventive medicine.

Authors:  C H Scriver
Journal:  Am J Public Health       Date:  1983-03       Impact factor: 9.308

Review 5.  X-linked hypophosphataemia: a homologous phenotype in humans and mice with unusual organ-specific gene dosage.

Authors:  C R Scriver; H S Tenenhouse
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

6.  Effect of the X-linked Hyp mutation on N-ethylmaleimide labelling of proteins in renal brush border membrane.

Authors:  E J Vizel; H S Tenenhouse; C R Scriver
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

Review 7.  Window panes of eternity. Health, disease, and inherited risk.

Authors:  C R Scriver
Journal:  Yale J Biol Med       Date:  1982 Sep-Dec
  7 in total

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