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New clinical genetics /

Sparad:
Bibliografiska uppgifter
Huvudupphovsman: Read, Andrew
Materialtyp: Bok
Språk:Spanish
Publicerad: Scion, 2011
Upplaga:2
Ämnen:
ADN
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008 000000b2011 |||||||| |||| 00| 0 spa d
020 |a 978-1-904842-80-4 
040 |a ULACIT  |c ULACIT 
050 |a MEDBC-2 002 
100 |a Read, Andrew  |9 10977 
245 |a New clinical genetics /  |c Andrew Read, Dian Donnai 
250 |a 2 
260 |b Scion,  |c 2011 
300 |a 450 p. 
505 |a What can we learn from a family history? How can a patient's chromosomes be studied? How do genes work? How can a patient's DNA be studied? How can we check a patient's DNA for gene mutations? What do mutations do? What is epigenetics? How do genes affect our metabolism, drug responses and immune system? How do researchers identify genes for mendelian diseases? Why are some conditions common and others rare? When is screening useful? Is cancer genetic? Should we be testing for genetic susceptibility to common diseases? What services are available for families with genetic disorders? Guidance for self-assessment questions 
600 |a Donnai Dian  |9 4035 
650 |a ADN  |9 15856 
650 |a ENFERMEDADES  |9 18184 
650 |a EPIGENETICA  |9 18285 
650 |a GENES  |9 18848 
650 |a GENETICA 
650 |a MEDICINA  |9 20038 
650 |a MUTACIONES GENETICAS  |9 20351 
650 |a NOV11  |9 20467 
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999 |c 12855  |d 12855 
952 |0 0  |1 0  |4 0  |7 0  |8 1  |9 14006  |a 1  |b 1  |d 2011-11-21  |l 0  |p 040413  |r 2022-09-05  |t 1  |w 2022-09-05  |y 1