Ich stimme zu, dass diese Seite Cookies verwende. Weitere Informationen finden Sie unter unseren Datenschutzerklärungen .
X
Kernohan, K.D.
89  Ergebnisse:
Personensuche X
?
1

A splice site and copy number variant responsible for TTC25..:

Backman, K. ; Mears, W.E. ; Waheeb, A....
European Journal of Medical Genetics.  64 (2021)  5 - p. 104193 , 2021
Link: https://doi.org/10.1016/..
 
?
2

A ZPR1 mutation is associated with a novel syndrome of grow..:

Ito, Y.A. ; Smith, A.C. ; Kernohan, K.D....
Clinical Genetics.  94 (2018)  3-4 - p. 303-312 , 2018
Link: https://doi.org/10.1111/..
 
?
3

Loss of the arginine methyltranserase PRMT7 causes syndromi..:

Kernohan, K.D. ; McBride, A. ; Xi, Y....
Clinical Genetics.  91 (2016)  5 - p. 708-716 , 2016
Link: https://doi.org/10.1111/..
 
?
4

ISDN2014_0391: CTCF is required to prevent p53‐ and PUMA‐de..:

Watson, L.A. ; Wang, X. ; Elbert, A...
International Journal of Developmental Neuroscience.  47 (2015)  Part_A - p. 115-115 , 2015
Link: https://doi.org/10.1016/..
 
?
5

The Impact of the United Nations on Poverty, Ignorance, and..:

Kernohan, Frances K.
Social Service Review.  29 (1955)  1 - p. 14-19 , 1955
Link: https://www.jstor.org/st..
 
?
6

Organization for Foreign Social Policy:

Kernohan, Frances K.
Social Work Journal.  34 (1953)  4 - p. 147-176 , 1953
Link: https://www.jstor.org/st..
 
?
7

Histone H3.3 beyond cancer: Germline mutations in Histone 3..:

Bryant, L ; Li, D ; Cox, S.G...
info:eu-repo/semantics/altIdentifier/doi/10.1126/sciadv.abc9207.  , 2020
Link: https://push-zb.helmholt..
 
?
8

PDXK mutations cause polyneuropathy responsive to pyridoxal..:

Chelban V ; Wilson M. P ; Warman Chardon J...
info:eu-repo/semantics/altIdentifier/pmid/31187503.  , 2019
Link: http://hdl.handle.net/10..
 
?
9

Runoff water quality from an urban catchment (Karama, Darwi..:

Kernohan, A.K ; Townsend, S.A
11/2000.  , 2018
Link: http://hdl.handle.net/10..
 
?
10

De Novo Truncating Mutations in WASF1 Cause Intellectual Di..:

Ito, Y ; Carss, K.J ; Duarte, S.T...
https://eprints.whiterose.ac.uk/143926/1/De%20Novo%20Truncating%20Mutations%20in%20WASF1%20Cause%20Intellectual%20Disability%20with%20Seizures.pdf.  , 2018
Link: https://eprints.whiteros..
 
?
11

Alternative genomic diagnoses for individuals with a clinic..:

Dyment, D. A. (David A.) ; O'Donnell-Luria, A. (Anne) ; Agrawal, P. B. (Pankaj B.)... , 2021
Link: http://urn.fi/urn:nbn:fi..
 
?
12

Histone H3.3 beyond cancer: Germline mutations in Histone 3..:

Bryant, L. (Laura) ; Li, D. (Dong) ; Cox, S.G. (Samuel G.)...
http://repub.eur.nl/pub/132337.  , 2020
Link: http://repub.eur.nl/pub/..
 
?
13

Dual effect of CTCF loss on neuroprogenitor differentiation..:

Watson, L.A. (L. Ashley) ; Wang, X. (Xu) ; Elbert, A. (Adrienne)...
http://repub.eur.nl/pub/74910.  , 2014
Link: http://repub.eur.nl/pub/..
 
?
14

Study protocol: optical coherence tomography angiography fo..:

Niestrata, Magdalena ; Deeks, Jonathan J ; Takwoingi, Yemisi...
BMJ Open.  14 (2024)  5 - p. e070857 , 2024
Link: https://doi.org/10.1136/..
 
?
15

RNA sequencing resolves novel DYNC2H1 variants causing shor..:

Marshall, Aren E. ; MacDonald, Stella K. ; Liang, Yijing...
Molecular Genetics & Genomic Medicine.  11 (2023)  10 - p. , 2023
Link: https://doi.org/10.1002/..
 
1-15