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X
Hejtmancik, JF
8  Ergebnisse:
Personensuche X
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1

Mutational spectrum in Usher syndrome type II:

Ouyang, XM ; Yam, D ; Hejtmancik, JF...
Clinical Genetics.  65 (2004)  4 - p. 288-293 , 2004
Link: https://doi.org/10.1046/..
 
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2

USH1C: a rare cause of USH1 in a non‐Acadian population and..:

Ouyang, XM ; Hejtmancik, JF ; Jacobson, SG...
Clinical Genetics.  63 (2003)  2 - p. 150-153 , 2003
Link: https://doi.org/10.1046/..
 
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3

Linkage and candidate gene analysis of autosomal‐dominant f..:

Shastry, BS ; Hejtmancik, JF ; Hiraoka, M...
Clinical Genetics.  58 (2000)  4 - p. 329-332 , 2000
Link: https://doi.org/10.1034/..
 
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4

Evidence for a neurologic defect in the men 2A/cutaneous li..:

Robinson, MF ; Furst, EJ ; Nunziata, V...
Bone and Mineral.  17 (1992)  - p. 91 , 1992
Link: https://doi.org/10.1016/..
 
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5

Mutation in the intracellular chloride channel CLCC1 associ..:

Li, L ; Jiao, X ; D'Atri, I...
https://discovery.ucl.ac.uk/id/eprint/10056583/1/Lin%20Li_Mutation.pdf.  , 2018
Link: https://discovery.ucl.ac..
 
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6

exomeSuite: Whole exome sequence variant filtering tool for..:

Maranhao, B ; Biswas, P ; Duncan, JL...
qt7439t013.  , 2014
Link: https://escholarship.org..
 
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7

Genetics of human cataract:

Shiels, A ; Hejtmancik, JF
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991604.  , 2013
Link: http://www.ncbi.nlm.nih...
 
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8

EPHA2 Polymorphisms and Age-Related Cataract in India:

Sundaresan, P ; Ravindran, RD ; Vashist, P...
https://researchonline.lshtm.ac.uk/id/eprint/20697/1/pone.0033001.pdf.  , 2012
Link: https://researchonline.l..
 
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