|
|
|
|
| LEADER |
00000cam a2200000 c 4500 |
| 001 |
1561438464 |
| 003 |
DE-627 |
| 005 |
20240507204148.0 |
| 007 |
tu |
| 008 |
170801s2015 xx ||||| m 00| ||eng c |
| 035 |
|
|
|a (DE-627)1561438464
|
| 035 |
|
|
|a (DE-576)49143846X
|
| 035 |
|
|
|a (DE-599)BSZ49143846X
|
| 035 |
|
|
|a (OCoLC)1010952906
|
| 040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rda
|
| 041 |
|
|
|a eng
|
| 084 |
|
|
|a 33
|2 sdnb
|
| 100 |
1 |
|
|a Thormälen, Aenne Solvejg
|d 1990-
|e VerfasserIn
|0 (DE-588)1136884874
|0 (DE-627)893676179
|0 (DE-576)490905285
|4 aut
|
| 245 |
1 |
4 |
|a The contribution of rare genetic variants to the heritability of myocardial infarction
|b systematic functional characterization of LDL-receptor missense alleless identified through exome sequencing of large clinical cohorts
|c vorgelegt von Aenne Solvejg Thormählen
|
| 264 |
|
1 |
|a Heidelberg
|c 2015
|
| 300 |
|
|
|a vi, 131 Blätter
|b Illustrationen
|
| 336 |
|
|
|a Text
|b txt
|2 rdacontent
|
| 337 |
|
|
|a ohne Hilfsmittel zu benutzen
|b n
|2 rdamedia
|
| 338 |
|
|
|a Band
|b nc
|2 rdacarrier
|
| 502 |
|
|
|b Dissertation
|c Ruprecht-Karls-Universität Heidelberg
|d 2017
|
| 583 |
1 |
|
|a Archivierung/Langzeitarchivierung gewährleistet
|f DISS
|x XA-DE-BW
|2 pdager
|5 DE-16
|
| 655 |
|
7 |
|a Hochschulschrift
|0 (DE-588)4113937-9
|0 (DE-627)105825778
|0 (DE-576)209480580
|2 gnd-content
|
| 751 |
|
|
|a Heidelberg
|0 (DE-588)4023996-2
|0 (DE-627)106300814
|0 (DE-576)208952578
|4 uvp
|
| 951 |
|
|
|a BO
|
| 992 |
|
|
|a 20170807
|
| 993 |
|
|
|a Thesis
|
| 994 |
|
|
|a 2017
|
| 998 |
|
|
|g 1136884874
|a Thormählen, Aenne Solvejg
|m 1136884874:Thormählen, Aenne Solvejg
|d 50000
|d 51001
|e 50000PT1136884874
|e 51001PT1136884874
|k 0/50000/
|k 1/50000/51001/
|p 1
|x j
|y j
|
| 999 |
|
|
|a KXP-PPN1561438464
|e 2976564566
|
| BIB |
|
|
|a Y
|
| JSO |
|
|
|a {"physDesc":[{"extent":"vi, 131 Blätter","noteIll":"Illustrationen"}],"type":{"bibl":"thesis"},"language":["eng"],"recId":"1561438464","origin":[{"publisherPlace":"Heidelberg","dateIssuedDisp":"2015","dateIssuedKey":"2015"}],"title":[{"subtitle":"systematic functional characterization of LDL-receptor missense alleless identified through exome sequencing of large clinical cohorts","title":"The contribution of rare genetic variants to the heritability of myocardial infarction","title_sort":"contribution of rare genetic variants to the heritability of myocardial infarction"}],"id":{"eki":["1561438464"]},"noteThesis":["Dissertation. - Ruprecht-Karls-Universität Heidelberg. - 2017"],"name":{"displayForm":["vorgelegt von Aenne Solvejg Thormählen"]},"person":[{"roleDisplay":"VerfasserIn","display":"Thormälen, Aenne Solvejg","role":"aut","family":"Thormälen","given":"Aenne Solvejg"}]}
|
| SRT |
|
|
|a THORMAELENCONTRIBUTI2015
|
