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Search Results - Damjanovich, Kristy
Search Results - Damjanovich, Kristy
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MHC Heterozygosity Confers a Selective Advantage against Multiple-Strain Infections
by
Penn, Dustin J.
,
Damjanovich, Kristy
,
Potts, Wayne K.
Published in
Proceedings of the National Academy of Sciences - PNAS
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5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasia
by
Damjanovich, Kristy
,
Langa, Carmen
,
Blanco, Francisco J
,
McDonald, Jamie
,
Botella, Luisa M
,
Bernabeu, Carmelo
,
Wooderchak-Donahue, Whitney
,
Stevenson, David A
,
Bayrak-Toydemir, Pinar
Published in
Orphanet journal of rare diseases
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Major Histocompatibility Complex Heterozygosity Reduces Fitness in Experimentally Infected Mice
by
Ilmonen, Petteri
,
Penn, Dustin J
,
Damjanovich, Kristy
,
Morrison, Linda
,
Ghotbi, Laleh
,
Potts, Wayne K
Published in
Genetics (Austin)
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A novel X‐linked multiple congenital anomaly syndrome associated with an EBP mutation
by
Furtado, Larissa V.
,
Bayrak‐Toydemir, Pinar
,
Hulinsky, Becki
,
Damjanovich, Kristy
,
Carey, John C.
,
Rope, Alan F.
Published in
American journal of medical genetics. Part A
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Novel Homozygous CYP1B1 Deletion in Siblings with Primary Congenital Glaucoma
by
Damjanovich, Kristy
,
Baldwin, Erin E.
,
Lewis, Tracey
,
Bayrak-Toydemir, Pinar
Published in
Ophthalmic genetics
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Infection-dependent phenotypes in MHC-congenic mice are not due to MHC: can we trust congenic animals?
by
McClelland, Erin E
,
Damjanovich, Kristy
,
Gardner, Kyle
,
Groesbeck, Zack J
,
Ma, Maggie S
,
Nibley, Megan
,
Richardson, Kelly S
,
Wilkinson, Maureen
,
Morrison, Linda C
,
Bernhardt, Paul
,
Potts, Wayne K
Published in
BMC immunology
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Unlabeled Oligonucleotides as Internal Temperature Controls for Genotyping by Amplicon Melting
by
Seipp, Michael T
,
Durtschi, Jacob D
,
Liew, Michael A
,
Williams, Jamie
,
Damjanovich, Kristy
,
Pont-Kingdon, Genevieve
,
Lyon, Elaine
,
Voelkerding, Karl V
,
Wittwer, Carl T
Published in
The Journal of molecular diagnostics : JMD
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p.R672C Mutation of MYH3 Gene in an Egyptian Infant Presented with Freeman-Sheldon Syndrome
by
Al-Haggar, Mohammad
,
Yahia, Soheir
,
Damjanovich, Kristy
,
Ahmad, Nermin
,
Hamada, Iman
,
Bayrak-Toydemir, Pinar
Published in
Indian journal of pediatrics
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Mosaicism in Stickler syndrome
by
Stevenson, David A
,
Vanzo, Rena
,
Damjanovich, Kristy
,
Hanson, Heather
,
Muntz, Harlan
,
Hoffman, Robert O
,
Bayrak-Toydemir, Pinar
Published in
European journal of medical genetics
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Inconsistent Results With Different Secondary Reflex Assays for Resolving HER2 Status
by
Willmore-Payne, Carlynn
,
Damjanovich-Colmenares, Kristy
,
Pasi, Alexandra V.
,
Werner, Theresa L.
,
Gulbahce, H. Evin
,
Downs-Kelly, Erinn
,
Geiersbach, Katherine B.
Published in
American journal of clinical pathology
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Novel homozygous CYP1B1 deletion in siblings with primary congenital glaucoma
by
Damjanovich, Kristy
,
Baldwin, Erin E
,
Lewis, Tracey
,
Bayrak-Toydemir, Pinar
Published in
Ophthalmic genetics
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A novel X-linked multiple congenital anomaly syndrome associated with an EBP mutation
by
Furtado, Larissa V.
,
Bayrak-Toydemir, Pinar
,
Hulinsky, Becki
,
Damjanovich, Kristy
,
Carey, John C.
,
Rope, Alan F.
Published in
American Journal of Medical Genetics Part A
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