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1
PCR detection of the TaqA RFLP at the DRD2 locus
PCR detection of the TaqA RFLP at the DRD2 locus
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PCR detection of the TaqA RFLP at the DRD2 locus

Grandy, D.K. ; Zhang, Y. ; Civelli, O.

Human molecular genetics, 1993-12, Vol.2 (12), p.2197-2197 [Periódico revisado por pares]

Oxford: Oxford University Press

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2
Linkage of the MHC to Familial Multiple Sclerosis Suggests Genetic Heterogeneity
Linkage of the MHC to Familial Multiple Sclerosis Suggests Genetic Heterogeneity
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Linkage of the MHC to Familial Multiple Sclerosis Suggests Genetic Heterogeneity

Haines, Jonathan L. ; Terwedow, Henry A. ; Burgess, Katie ; Pericak-Vance, Margaret A. ; Rimmler, Jackie B. ; Martin, Eden R. ; Oksenberg, Jorge R. ; Lincoln, Robin ; Zhang, David Y. ; Banatao, Diosdado R. ; Gatto, Nicole ; Goodkin, Donald E. ; Hauser, Stephen L.

Human molecular genetics, 1998-08, Vol.7 (8), p.1229-1234 [Periódico revisado por pares]

Oxford University Press

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3
Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson—Weiss syndrome
Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson—Weiss syndrome
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Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson—Weiss syndrome

Gorry, Michael C. ; Preston, Robert A. ; White, Gregory J. ; Zhang, Yingze ; Singhal, Virender K. ; Losken, H.Wolgang ; Parker, Michael G. ; Nwokoro, Ngozi A. ; Post, J.Christopher ; Ehrlich, Garth D.

Human molecular genetics, 1995-08, Vol.4 (8), p.1387-1390 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity : The multiple sclerosis genetics group
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity : The multiple sclerosis genetics group
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Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity : The multiple sclerosis genetics group

HAINES, J. L ; TERWEDOW, H. A ; GATTO, N ; GOODKIN, D. E ; HAUSER, S. L ; BURGESS, K ; PERICAK-VANCE, M. A ; RIMMLER, J. B ; MARTIN, E. R ; OKSENBERG, J. R ; LINCOLN, R ; ZHANG, D. Y ; BANATAO, D. R

Human molecular genetics, 1998-08, Vol.7 (8), p.1229-1234 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Temperature-Sensitive Mutation in PEX1 Moderates the Phenotypes of Peroxisome Deficiency Disorders
Temperature-Sensitive Mutation in PEX1 Moderates the Phenotypes of Peroxisome Deficiency Disorders
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Temperature-Sensitive Mutation in PEX1 Moderates the Phenotypes of Peroxisome Deficiency Disorders

Imamura, Atsushi ; Tamura, Shigehiko ; Shimozawa, Nobuyuki ; Suzuki, Yasuyuki ; Zhang, Zhongyi ; Tsukamoto, Toshiro ; Orii, Tadao ; Kondo, Naomi ; Osumi, Takashi ; Fujiki, Yukio

Human molecular genetics, 1998-12, Vol.7 (13), p.2089-2094 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
Insulin-Dependent Diabetes Mellitus (IDDM) Is Associated with CTLA4 Polymorphisms in Multiple Ethnic Groups
Insulin-Dependent Diabetes Mellitus (IDDM) Is Associated with CTLA4 Polymorphisms in Multiple Ethnic Groups
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Insulin-Dependent Diabetes Mellitus (IDDM) Is Associated with CTLA4 Polymorphisms in Multiple Ethnic Groups

Marron, Michele P. ; Raffel, Leslie J. ; Garchon, Henri-Jean ; Jacob, Chaim O. ; Serrano-Rios, Manuel ; Martinez Larrad, Maria T. ; Teng, Wei-Ping ; Park, Yongsoo ; Zhang, Zhi-Xing ; Goldstein, Darlene R. ; Tao, Yi-Wen ; Beaurain, Genevieve ; Bach, Jean-Francois ; Huang, Hong-So ; Luo, De-Fang ; Zeidler, Adina ; Rotter, Jerome I. ; Yang, Mark C. K. ; Modilevsky, Tamara ; Maclaren, Noel K. ; She, Jin-Xiong

Human molecular genetics, 1997-08, Vol.6 (8), p.1275-1282 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
Molecular isolation and characterization of an expressed gene from the human Y chromosome
Molecular isolation and characterization of an expressed gene from the human Y chromosome
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Molecular isolation and characterization of an expressed gene from the human Y chromosome

Zhang, Julie S. ; Yang-Feng, Teresa L. ; Muller, Ulrich ; Mohandas, T.K. ; de Jong, Pieter J. ; Lau, Yan-Fai Chris

Human molecular genetics, 1992-12, Vol.1 (9), p.717-726 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin α2-Chain
Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin α2-Chain
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Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin α2-Chain

Allamand, Valérie ; Sunada, Yoshihide ; Salih, Mustafa A. M. ; Straub, Volker ; Ozo, O. ; Al-Turaiki, M. H. S. ; Akbar, Maksood ; Kolo, Timo ; Colognato, Holly ; Zhang, Xu ; Sorokin, Lydia M. ; Yurchenco, Peter D. ; Tryggvason, Karl ; Campbell, Kevin P.

Human molecular genetics, 1997-05, Vol.6 (5), p.747-752 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha 2-chain
Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha 2-chain
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Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha 2-chain

Allamand, V ; Sunada, Y ; Salih, MAM ; Straub, V ; Ozo, C O ; Al-Turaiki, MHS ; Akbar, M ; Kolo, T ; Campbell, K P

Human molecular genetics, 1997-05, Vol.6 (5), p.747-752 [Periódico revisado por pares]

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10
Compost and compost water extract-induced systemic acquired resistance in cucumber and Arabidopsis
Compost and compost water extract-induced systemic acquired resistance in cucumber and Arabidopsis
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Compost and compost water extract-induced systemic acquired resistance in cucumber and Arabidopsis

Zhang, W ; Han, D Y ; Dick, WA ; Davis, K R ; Hoitink, HAJ

Human molecular genetics, 1998-07, Vol.7 (7), p.450-455 [Periódico revisado por pares]

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