Results 231 to 240 of about 227,732 (266)
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The Inherited Neuropathies

Neurologic Clinics, 2007
Neuropathy is one of the most common referrals to neurologic clinics. Patients often undergo extensive testing for acquired etiologies; inherited causes are common. Increasingly, genetic causes are becoming known and commercial testing available. The rate of recent discovery has been rapid and relates to the extent of single gene disorders of nerve ...
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Inheritance in Lettuce

Science, 1929
Bibliography: p. 339-341. ; Made available in DSpace on 2007-11-07T15:41:50Z (GMT). No. of bitstreams: 1 inheritanceinlet00durs.pdf: 8034294 bytes, checksum: faac72354d494394504ab30e10ad661f (MD5) Previous issue date: 1930 ; Cover title. ; """The results presented in this bulletin form part of a thesis submitted by the author to the Graduate School of ...
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Inheritance

Science, 1967
W H, Finley, S C, Finley
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Inheritance of hypophosphatasia

Medical Hypotheses, 1985
A system of multiple, codominant alleles (HN, HC, HI) is proposed for the inheritance of hypophosphatasia. These alleles are associated with a single autosomal locus which determines the presence or absence of hypophosphatasia among human subjects. Either HC or HI conditions hypophosphatasia whereas HN conditions the absence of this disorder.
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Inherited myotonias

The inherited myotonias are a complex group of diseases caused by variations in genes that encode or modulate the expression of ion channels that regulate muscle excitability. These variations alter muscle membrane excitability allowing mild depolarization, causing myotonic discharges.
Karen, Suetterlin   +2 more
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Epigenetic inheritance and reproductive mode in plants and animals

Trends in Ecology and Evolution, 2021
Maren Wellenreuther   +2 more
exaly  

Inherited Neuropathies

Mayo Clinic Proceedings, 1983
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Digging the channels of inheritance: On how to distinguish between cultural and biological inheritance

Philosophical Transactions of the Royal Society B: Biological Sciences, 2021
Maria Kronfeldner
exaly  

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