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Leader
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00000cz a2200037n 45 0 |
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001
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NII|DA0114676X
(VIAF cluster)
(Authority/Source Record)
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005
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20230615104433.0 |
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003
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NII |
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008
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230615nneanz||abbn n and d |
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035
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‡a
(NII)DA0114676X
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100
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1 |
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‡a
Porter, Ian H.
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670
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‡a
Author of Human embryonic and fetal death
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670
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‡a
Author of Heredity and disease
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919
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‡a
heredityanddisease
‡A
Heredity and disease
‡9
1
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919
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‡a
humanembryonicandfetaldeath
‡A
Human embryonic and fetal death
‡9
1
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996
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‡2
BNF|15106718
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996
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‡2
RERO|A003706271
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996
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‡2
DNB|1220231118
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996
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‡2
WKP|Q5982611
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996
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‡2
NTA|10041107X
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996
|
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‡2
LC|no2019056946
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996
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‡2
ISNI|0000000084493041
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|
996
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‡2
WKP|Q47347273
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|
996
|
|
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‡2
DNB|1062012321
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996
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‡2
CAOONL|ncf10111256
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996
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‡2
NTA|067787215
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|
996
|
|
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‡2
BNF|12269320
|
|
996
|
|
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‡2
ISNI|0000000081071820
|
|
996
|
|
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‡2
LC|no2016077505
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996
|
|
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‡2
RERO|A026589989
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|
996
|
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‡2
WKP|Q94662316
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|
996
|
|
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‡2
DNB|1220232696
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|
996
|
|
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‡2
ISNI|0000000074295172
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996
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‡2
WKP|Q16196218
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996
|
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‡2
J9U|987007521172105171
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996
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‡2
PLWABN|9810579192405606
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|
996
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‡2
ISNI|000000038366412X
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|
996
|
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‡2
LC|n 2018058038
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996
|
|
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‡2
BIBSYS|90553792
|
|
996
|
|
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‡2
J9U|987007340699105171
|
|
996
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‡2
PLWABN|9813923182105606
|
|
996
|
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‡2
WKP|Q124629241
|
|
996
|
|
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‡2
NUKAT|n 00067777
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|
996
|
|
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‡2
PLWABN|9810649990305606
|
|
996
|
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‡2
SUDOC|160726026
|
|
996
|
|
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‡2
WKP|Q92815803
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|
996
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|
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‡2
BIBSYS|90906251
|
|
996
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|
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‡2
N6I|vtls000038943
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996
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‡2
DNB|1173361405
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|
996
|
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‡2
LC|no2024030421
|
|
996
|
|
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‡2
CAOONL|ncf10334153
|
|
996
|
|
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‡2
SUDOC|251035654
|
|
996
|
|
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‡2
J9U|987007345107905171
|
|
996
|
|
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‡2
WKP|Q3807704
|
|
996
|
|
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‡2
BIBSYS|90774535
|
|
996
|
|
|
‡2
NTA|071868615
|
|
996
|
|
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‡2
RERO|A003706262
|
|
996
|
|
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‡2
NTA|070256853
|
|
996
|
|
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‡2
WKP|Q58797387
|
|
996
|
|
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‡2
LC|n 90612593
|
|
996
|
|
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‡2
WKP|Q30122391
|
|
996
|
|
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‡2
LC|n 86808862
|
|
996
|
|
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‡2
BNF|12361886
|
|
996
|
|
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‡2
DNB|137969279
|
|
996
|
|
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‡2
WKP|Q105666468
|
|
996
|
|
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‡2
CAOONL|ncf10446698
|
|
996
|
|
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‡2
ISNI|000000038803096X
|
|
996
|
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‡2
J9U|987007318520605171
|
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996
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‡2
NTA|227922638
|
|
996
|
|
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‡2
ISNI|0000000072866664
|
|
996
|
|
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‡2
ISNI|0000000043651031
|
|
996
|
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‡2
ISNI|0000000076740284
|
|
996
|
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‡2
ISNI|0000000083540870
|
|
996
|
|
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‡2
LC|nb2009029479
|
|
996
|
|
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‡2
WKP|Q20657599
|
|
996
|
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‡2
WKP|Q17198450
|
|
996
|
|
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‡2
NKC|xx0026990
|
|
996
|
|
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‡2
NUKAT|n 2021144417
|
|
996
|
|
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‡2
DNB|1074252675
|
|
996
|
|
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‡2
BIBSYS|6067731
|
|
996
|
|
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‡2
LC|nb 99160834
|
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996
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‡2
WKP|Q106536159
|
|
996
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‡2
LC|n 90677589
|
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997
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‡a
0 0 lived 0 0
‡9
1
|
|
998
|
|
|
‡a
Porter, Ian H.
‡2
DNB|1220231118
‡3
exact name
|
|
998
|
|
|
‡a
Porter, Ian H
‡2
NLA|000035429142
‡3
exact name
|
|
998
|
|
|
‡a
Porter, Ian H.
‡2
BIBSYS|90222604
‡3
viafid
‡3
exact title: (1.00, 'humanembryonicandfetaldeath', 'humanembryonicandfetaldeath')
|
|
998
|
|
|
‡a
Porter, Ian H
‡2
RERO|A003706262
‡3
exact name
|
|
998
|
|
|
‡a
Porter, Ian H.
‡2
LC|n 79055876
‡3
exact title: (1.00, 'heredityanddisease', 'heredityanddisease')
|
|
998
|
|
|
‡a
Porter, Ian H.
‡2
SUDOC|085136646
‡3
exact title: (1.00, 'humanembryonicandfetaldeath', 'humanembryonicandfetaldeath')
|
|
998
|
|
|
‡a
Porter, Ian H.
‡2
NUKAT|n 2021144417
‡3
viafid
|
|
998
|
|
|
‡a
Porter, Ian H.
‡2
NTA|067787215
‡3
exact name
|
|
998
|
|
|
‡a
Porter, Ian H.
‡2
J9U|987007345107905171
‡3
viafid
|
|
998
|
|
|
‡a
Porter, Ian H.
‡2
ISNI|0000000084493041
‡3
exact name
|
