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Lowe, Mundell
16  Ergebnisse:
Personensuche X
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1

World's greatest jazz solos 

guitar 
Lowe, Mundell , 1978
Exemplar:  Zentrale:Magazinturm-E02 a not 609 jaz/78
 
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2

MUNDELL LOWE AND HIS ALL STARS: More TV Action Jazz! 

Naxos Music Library Jazz
Lowe, Mundell ; Duning, George ; Livingston, Jerry... , 1960
Link: http://suub.naxosmusicli..
 
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3

MUNDELL LOWE QUARTET: MUNDELL LOWE QUARTET 

Naxos Music Library Jazz
Malneck, Matty ; Signorelli, Frank ; Lowe, Mundell... ,
Link: http://suub.naxosmusicli..
 
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4

LOWE, Mundell / Wells, Lloyd: This One's for Charlie 

Naxos Music Library Jazz
Schertzinger, Victor ; Berlin, Irving ; Mandel, Johnny... ,
Link: http://suub.naxosmusicli..
 
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5

Rare missense variants in Tropomyosin‐4 (TPM4) are associat..:

Stapley, Rachel J. ; Poulter, Natalie S. ; Khan, Abdullah O....
Journal of Thrombosis and Haemostasis.  20 (2022)  2 - p. 478-485 , 2022
Link: https://doi.org/10.1111/..
 
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6

A novel mutation in the P2Y12receptor and a function-reduci..:

Patel, Y. M. ; Lordkipanidzé, M. ; Lowe, G. C....
Journal of Thrombosis and Haemostasis.  12 (2014)  5 - p. 716-725 , 2014
Link: https://doi.org/10.1111/..
 
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7

Charlie Parker live vol. 2 

, In: Bebop story
1950 & 52 
Parker, Charlie ; Hyman, Dick ; Lowe, Mundell.... (2008)  87
Exemplar:  Zentrale/Mediathek: pd 6359-4
 
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8

Rare missense variants in Tropomyosin-4 (TPM4) are associat..:

Stapley, RJ ; Poulter, NS ; Khan, AO...
https://discovery.ucl.ac.uk/id/eprint/10152651/1/J%20of%20Thrombosis%20Haemost%20-%202021.pdf.  , 2022
Link: https://discovery.ucl.ac..
 
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9

Whole exome sequencing identifies genetic variants in inher..:

Johnson, Ben ; Lowe, Gillian C ; Futterer, Jane...
Johnson , B , Lowe , G C , Futterer , J , Lordkipanidzé , M , Macdonald , D , Simpson , M A , Sanchez-Guiú , I , Drake , S , Bem , D , Leo , V , Fletcher , S J , Dawood , B , Rivera , J , Allsup , D , Biss , T , Bolton-Maggs , P H , Collins , P , Curry , N , Grimley , C , James , B , Makris , M , Motwani , J , Pavord , S , Talks , K , Thachil , J , Wilde , J , Williams , M , Harrison , P , Gissen , P , Mundell , S , Mumford , A , Daly , M E , Watson , S P & Morgan , N V 2016 , ' Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects ' , Haematologica , vol. 101 , no. 10 , pp. 1170-1179 . https://doi.org/10.3324/haematol.2016.146316.  , 2016
Link: https://kclpure.kcl.ac.u..
 
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10

Whole exome sequencing identifies genetic variants in inher..:

Johnson, Ben ; Lowe, Gillian C ; Futterer, Jane...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046646/.  , 2016
Link: http://www.ncbi.nlm.nih...
 
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11

Whole exome sequencing identifies genetic variants in inher..:

Johnson, Ben ; Lowe, Gillian C ; Futterer, Jane...
Johnson , B , Lowe , G C , Futterer , J , Lordkipanidzé , M , Macdonald , D , Simpson , M A , Sanchez-Guiú , I , Drake , S , Bem , D , Leo , V , Fletcher , S J , Dawood , B , Rivera , J , Allsup , D , Biss , T , Bolton-Maggs , P H , Collins , P , Curry , N , Grimley , C , James , B , Makris , M , Motwani , J , Pavord , S , Talks , K , Thachil , J , Wilde , J , Williams , M , Harrison , P , Gissen , P , Mundell , S , Mumford , A , Daly , M E , Watson , S P & Morgan , N V 2016 , ' Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects ' , Haematologica , vol. 101 , no. 10 , pp. 1170-1179 . https://doi.org/10.3324/haematol.2016.146316.  , 2016
Link: https://kclpure.kcl.ac.u..
 
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12

Whole exome sequencing identifies genetic variants in inher..:

Johnson, B ; Lowe, G. C ; Futterer, J...
https://hull-repository.worktribe.com/output/752220.  , 2016
Link: https://hull-repository...
 
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13

Whole Exome Sequencing Identifies Genetic Variants In Inher..:

Johnson, Ben ; Lowe, Gillian C ; Futterer, Jane...
Johnson , B , Lowe , G C , Futterer , J , Lordkipanidze' , M , MacDonald , D , Simpson , M A , Sanchez Guiu' , I , Drake , S , Bem , D , Leo , V , Fletcher , S J , Dawood , B , Rivera , J , Allsup , D , Biss , T , Bolton-Maggs , P H B , Collins , P , Curry , N , Grimley , C , James , B , Makris , M , Motwani , J , Pavord , S , Talks , K , Thachil , J , Wilde , J , Williams , M , Harrison , P , Gissen , P , Mundell , S J , Mumford , A , Daly , M E , Watson , S P , Morgan , N V 2016 , ' Whole Exome Sequencing Identifies Genetic Variants In Inherited Thrombocytopenia With Secondary Qualitative Function Defects ' , Haematologica , vol. 101 , no. 10 , pp. 1170-1179 . https://doi.org/10.3324/haematol.2016.146316.  , 2016
Link: https://hdl.handle.net/1..
 
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14

Whole exome sequencing identifies genetic variants in inher..:

Johnson, B ; Lowe, GC ; Futterer, J...
https://discovery.ucl.ac.uk/id/eprint/1524337/1/Gissen_1170.full.pdf.  , 2016
Link: https://discovery.ucl.ac..
 
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15

Diversity and impact of rare variants in genes encoding the..:

Jones, Matthew L ; Norman, Jane E ; Morgan, Neil V...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510585/.  , 2015
Link: http://www.ncbi.nlm.nih...
 
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