Ich stimme zu, dass diese Seite Cookies verwende. Weitere Informationen finden Sie unter unseren Datenschutzerklärungen .
X
Monaghan, K.G.
1101  Ergebnisse:
Personensuche X
?
1

Further evidence that de novo missense and truncating varia..:

Cohen, J.S. ; Srivastava, S. ; Farwell Hagman, K.D....
Clinical Genetics.  91 (2016)  5 - p. 697-707 , 2016
Link: https://doi.org/10.1111/..
 
?
2

ACMG statement on noninvasive prenatal screening for fetal ..:

Gregg, Anthony R. ; Gross, S.J. ; Best, R.G....
Genetics in Medicine.  15 (2013)  5 - p. 395-398 , 2013
Link: https://doi.org/10.1038/..
 
?
3

Is Cystic Fibrosis Carrier Screening Cost Effective?:

Wei, S. ; Quigg, M.H. ; Monaghan, K.G.
Community Genetics.  10 (2007)  2 - p. 103-109 , 2007
Link: https://www.jstor.org/st..
 
?
4

Genotype-phenotype correlation and frequency of the 3199del..:

Monaghan, K.G. ; Highsmith, W.E. ; Amos, J....
Genetics in Medicine.  6 (2004)  5 - p. 421-425 , 2004
Link: https://doi.org/10.1097/..
 
?
5

Prophylactic total gastrectomy for familial gastric cancer:

Lewis, F.R. ; Mellinger, J.D. ; Hayashi, A....
Surgery.  130 (2001)  4 - p. 612-619 , 2001
Link: https://doi.org/10.1067/..
 
?
6

Frequency and clinical significance of the S1235R mutation ..:

Monaghan, K.G. ; Feldman, G.L. ; Barbarotto, G.M....
American Journal of Medical Genetics.  95 (2000)  4 - p. 361-365 , 2000
Link: https://doi.org/10.1002/..
 
?
7

The frequency and clinical significance of the S1235R mutat..:

Feldman, G.L. ; Monaghan, K.G. ; Barbaratto, G.M..
Genetics in Medicine.  2 (2000)  1 - p. 104 , 2000
Link: https://doi.org/10.1097/..
 
?
8

Genetic analysis of patients with pancreatitis and a histor..:

Monaghan, K.G. ; Jackson, C.E. ; Feldman, G.L.
Genetics in Medicine.  1 (1999)  2 - p. 49 , 1999
Link: https://doi.org/10.1097/..
 
?
9

The risk of cystic fibrosis with prenatally detected echoge..:

Monaghan, K. G. ; Feldman, G. L.
Prenatal Diagnosis.  19 (1999)  7 - p. 604-609 , 1999
Link: https://doi.org/10.1002/..
 
?
10

Calcitonin in tissues of thyroidectomized monkey:

Becker, K. L. ; Geelhoed, G. ; O'Neill, W....
Experientia.  36 (1980)  5 - p. 609-610 , 1980
Link: https://doi.org/10.1007/..
 
?
11

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/..
 
?
12

Disruptive variants of CSDE1 associate with autism and inte..:

Guo, H. (Hui) ; Li, Y. (Ying) ; Shen, L. (Lu)...
http://repub.eur.nl/pub/119920.  , 2019
Link: http://repub.eur.nl/pub/..
 
?
13

Loss of UGP2 in brain leads to a severe epileptic encephalo..:

Perenthaler, E. (Elena) ; Nikoncuk, A. (Anita) ; Yousefi, S. (Soheil)...
http://repub.eur.nl/pub/122932.  , 2019
Link: http://repub.eur.nl/pub/..
 
?
14

De Novo Truncating Mutations in the Last and Penultimate Ex..:

Jansen, S. (Sandra) ; Geuer, S. (Sinje) ; Pfundt, R. (Rolph)...
http://repub.eur.nl/pub/98864.  , 2017
Link: http://repub.eur.nl/pub/..
 
?
15

Mutations in HIVEP2 are associated with developmental delay..:

Steinfeld, H. (Hallie) ; Cho, M.T. (Megan T.) ; Retterer, K. (Kyle)...
http://repub.eur.nl/pub/90974.  , 2016
Link: http://repub.eur.nl/pub/..
 
1-15