Von Hippel-Lindau Syndrome
Neumann, Hartmut P.H., Lips, Cornells J.M., Hsia, Y. Edward, Zbar, Berton
Published in Brain pathology (Zurich, Switzerland) (01.04.1995)
Published in Brain pathology (Zurich, Switzerland) (01.04.1995)
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Orthopaedic manifestations of Marinesco-Sjögren syndrome
Reinker, Kent, Hsia, Y Edward, Rimoin, David L, Henry, George, Yuen, Juliet, Powell, Berkley, Wilcox, William R
Published in Journal of pediatric orthopaedics (01.05.2002)
Published in Journal of pediatric orthopaedics (01.05.2002)
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Determination of the breakpoint of the common α‐thalassaemia deletion in Filipinos in Hawaii
Hunt, John A., Lee, Lara, Donlon, Timothy A., Hsia, Y. Edward
Published in British journal of haematology (01.02.1999)
Published in British journal of haematology (01.02.1999)
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Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype
Chen, F, Kishida, T, Yao, M, Hustad, T, Glavac, D, Dean, M, Gnarra, J R, Orcutt, M L, Duh, F M, Glenn, G
Published in Human mutation (1995)
Published in Human mutation (1995)
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Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma
WHALEY, J. M, NAGLICH, J, KLEIN-SZANTO, A. J. P, SEIZINGER, B. R, KLEY, N, GELBERT, L, HSIA, Y. E, LAMIELL, J. M, GREEN, J. S, COLLINS, D, NEUMANN, H. P. H, LAIDLAW, J, LI, F. P
Published in American journal of human genetics (01.12.1994)
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Published in American journal of human genetics (01.12.1994)
Journal Article
Desbuquois syndrome: clinical, radiographic, and morphologic characterization
Shohat, M, Lachman, R, Gruber, H E, Hsia, Y E, Golbus, M S, Witt, D R, Bodell, A, Bryke, C R, Hogge, W A, Rimoin, D L
Published in American journal of medical genetics (01.08.1994)
Published in American journal of medical genetics (01.08.1994)
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Near-total intestinal aganglionosis in the Waardenburg-Shah syndrome
Shim, Walton K.T, Derieg, Marta, Powell, Berkley R, Hsia, Y.Edward
Published in Journal of pediatric surgery (01.12.1999)
Published in Journal of pediatric surgery (01.12.1999)
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Frequency of glucose-6-phosphate dehydrogenase (G6PD) mutations in Chinese, Filipinos, and Laotians from Hawaii
Hsia, Y E, Miyakawa, F, Baltazar, J, Ching, N S, Yuen, J, Westwood, B, Beutler, E
Published in Human genetics (01.11.1993)
Published in Human genetics (01.11.1993)
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A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia: exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrix
Rimoin, D L, Rasmussen, I M, Briggs, M D, Roughley, P J, Gruber, H E, Warman, M L, Olsen, B R, Hsia, Y E, Yuen, J, Reinker, K
Published in Human genetics (01.03.1994)
Published in Human genetics (01.03.1994)
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Propionic acidemia: A clinical update
Wolf, Barry, Hsia, Y. Edward, Sweetman, Lawrence, Gravel, Roy, Harris, David J., Nyhan, William L.
Published in The Journal of pediatrics (01.12.1981)
Published in The Journal of pediatrics (01.12.1981)
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