A new approach to mutational analysis at the human phenylalanine hydroxylase locus: application of in-vitro-DNA-amplification to the study of mutations resulting in phenylalanine hydroxylase deficiency in man

Saved in:
Bibliographic Details
Main Author: Konecki, David S. (Author)
Format: Book/Monograph Thesis
Language:English
Published: 1989
Subjects:
Online Access: Get full text
Author Notes:vorgelegt von David S. Konecki

MARC

LEADER 00000cam a2200000 c 4500
001 1650804776
003 DE-627
005 20240510193446.0
007 tu
008 900530s1989 xx ||||| m 00| ||eng c
015 |a 90,H05,1399  |2 dnb 
016 7 |a 900632453  |2 DE-101 
035 |a (DE-627)1650804776 
035 |a (DE-576)020587988 
035 |a (DE-599)DNB900632453 
035 |a (OCoLC)75147701 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
084 |a 33  |2 sdnb 
084 |a 33  |2 sdnb 
084 |a XC 1604  |2 rvk  |0 (DE-625)rvk/152496:12910 
100 1 |a Konecki, David S.  |0 (DE-588)1140947494  |0 (DE-627)89878526X  |0 (DE-576)166571717  |4 aut 
245 1 2 |a A new approach to mutational analysis at the human phenylalanine hydroxylase locus  |b application of in-vitro-DNA-amplification to the study of mutations resulting in phenylalanine hydroxylase deficiency in man  |c vorgelegt von David S. Konecki 
264 1 |c 1989 
300 |a 174 Bl.  |b Ill., graph. Darst. 
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 |a Heidelberg, Univ., Diss., 1989 (Nicht f.d. Austausch) 
583 1 |a Archivierung prüfen  |c 20200919  |f DE-640  |z 1  |2 pdager 
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 
936 r v |a XC 1604  |b Dissertation, Habilitationsarbeit  |k Medizin  |k Allgemeine Medizin, Krankenhauswesen, Krankenpflege  |k Medizin, Allgemein  |k A. Formalschlüssel  |k Dissertation, Habilitationsarbeit  |0 (DE-627)1272479366  |0 (DE-625)rvk/152496:12910  |0 (DE-576)202479366 
951 |a BO 
992 |a 20171006 
993 |a Thesis 
994 |a 1989 
998 |g 1140947494  |a Konecki, David S.  |m 1140947494:Konecki, David S.  |d 50000  |d 51001  |e 50000PK1140947494  |e 51001PK1140947494  |k 0/50000/  |k 1/50000/51001/  |p 1  |x j  |y j 
999 |a KXP-PPN1650804776  |e 3338968906 
BIB |a Y 
JSO |a {"type":{"bibl":"thesis"},"physDesc":[{"extent":"174 Bl.","noteIll":"Ill., graph. Darst."}],"recId":"1650804776","language":["eng"],"name":{"displayForm":["vorgelegt von David S. Konecki"]},"person":[{"role":"aut","display":"Konecki, David S.","given":"David S.","family":"Konecki"}],"noteThesis":["Heidelberg, Univ., Diss., 1989 (Nicht f.d. Austausch)"],"title":[{"subtitle":"application of in-vitro-DNA-amplification to the study of mutations resulting in phenylalanine hydroxylase deficiency in man","title":"A new approach to mutational analysis at the human phenylalanine hydroxylase locus","title_sort":"new approach to mutational analysis at the human phenylalanine hydroxylase locus"}],"origin":[{"dateIssuedKey":"1989","dateIssuedDisp":"1989"}],"id":{"eki":["1650804776"]}} 
SRT |a KONECKIDAVNEWAPPROAC1989