E-LIB Suche - Ergebnisse für: Urquhart, Alfred E.

1

Fluorescent Vi Antibody Test in the Screening of Typhoid Ca..:

Chitkara, Yoginder K. ; Urquhart, Alfred E.
American Journal of Clinical Pathology. 72 (1979) 1 - p. 87-89 , 1979

2

Lettres adressées à Mgr Dupanloup par :. XII Dubard-Eymard:

Dupanloup, Monseigneur Félix-Antoine-Philibert. Producteur d'un fonds ; Dubard, Lieutenant Ferdinand. Auteur de lettres ; Hubault, Gustave. Auteur de lettres...
Notice du catalogue : http://archivesetmanuscrits.bnf.fr/ark:/12148/cc6402q/cd0e22424. ,

Link: http://gallica.bnf.fr/ar..

3

Lettres adressées à Mgr Dupanloup par :. XII Dubard-Eymard:

Dupanloup, Monseigneur Félix-Antoine-Philibert. Producteur d'un fonds ; Dubard, Lieutenant Ferdinand. Auteur de lettres ; Hubault, Gustave. Auteur de lettres...
Notice du catalogue : http://archivesetmanuscrits.bnf.fr/ark:/12148/cc6402q/cd0e22424. ,

Link: http://gallica.bnf.fr/ar..

4

Bi-allelic variants in the mitochondrial RNase P subunit PR..:

Hochberg, Irit ; Demain, Leigh A.M. ; Richer, Julie...
The American Journal of Human Genetics. 108 (2021) 11 - p. 2195-2204 , 2021

Link: https://doi.org/10.1016/..

5

Characterising a homozygous two‐exon deletion inUQCRH: comp..:

Vidali, Silvia ; Gerlini, Raffaele ; Thompson, Kyle...
EMBO Molecular Medicine. 13 (2021) 12 - p. , 2021

Link: https://doi.org/10.15252..

6

Enhanced Hyaluronan Signaling and Autophagy Dysfunction by ..:

Rahman, Abir A. ; Soto-Avellaneda, Alejandro ; Yong Jin, Hyun...
Neuroscience. 441 (2020) - p. 33-45 , 2020

Link: https://doi.org/10.1016/..

7

Ligase IV syndrome can present with microcephaly and radial..:

Madhu, Rajesh ; Beaman, Glenda M. ; Chandler, Kate E....
European Journal of Medical Genetics. 63 (2020) 9 - p. 103974 , 2020

Link: https://doi.org/10.1016/..

8

A homozygous missense variant in CHRM3 associated with fami..:

Beaman, Glenda M. ; Galatà, Gabriella ; Teik, Keng W....
Clinical Genetics. 96 (2019) 6 - p. 515-520 , 2019

Link: https://doi.org/10.1111/..

9

Variants in myelin regulatory factor (MYRF) cause autosomal..:

Garnai, Sarah J. ; Brinkmeier, Michelle L. ; Emery, Ben...
PLOS Genetics. 15 (2019) 5 - p. e1008130 , 2019

Link: https://doi.org/10.1371/..

10

Homozygous mutation in PTRH2 gene causes progressive sensor..:

Sharkia, Rajech ; Shalev, Stavit A. ; Zalan, Abdelnaser...
American Journal of Medical Genetics Part A. 173 (2017) 4 - p. 1051-1055 , 2017

Link: https://doi.org/10.1002/..

11

Erratum: Corrigendum: Mutations in SNORD118 cause the cereb..:

Jenkinson, Emma M ; Rodero, Mathieu P ; Kasher, Paul R...
Nature Genetics. 49 (2017) 2 - p. 317-317 , 2017

Link: https://doi.org/10.1038/..

12

Preface to the Special Issue on Applied Combinatorial Optim..:

Cancela, Héctor ; Martins, Simone ; Mauttone, Antonio.
International Transactions in Operational Research. 24 (2016) 1-2 - p. 3-5 , 2016

Link: https://doi.org/10.1111/..

13

Mutations in SNORD118 cause the cerebral microangiopathy le..:

Jenkinson, Emma M ; Rodero, Mathieu P ; Kasher, Paul R...
Nature Genetics. 48 (2016) 10 - p. 1185-1192 , 2016

Link: https://doi.org/10.1038/..

14

Oculo-auriculo-vertebral spectrum: Clinical and molecular a..:

Beleza-Meireles, Ana ; Hart, Rachel ; Clayton-Smith, Jill...
European Journal of Medical Genetics. 58 (2015) 9 - p. 455-465 , 2015

Link: https://doi.org/10.1016/..

15

Agnathia-otocephaly complex and asymmetric velopharyngeal i..:

Sergouniotis, Panagiotis I ; Urquhart, Jill E ; Williams, Simon G...
Journal of Human Genetics. 60 (2015) 4 - p. 199-202 , 2015

Link: https://doi.org/10.1038/..