Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
Belloni, E, Muenke, M, Roessler, E, Traverse, G, Siegel-Bartelt, J, Frumkin, A, Mitchell, H.F, Donis-Keller, H, Helms, C, Hing, A.V, Heng, H.H.Q, Koop, B, Martindale, D, Rommens, J.M, Tsui, L.-C, Scherer, S.W
Published in Nature genetics (01.11.1996)
Published in Nature genetics (01.11.1996)
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Journal Article
Physical mapping of the holoprosencephaly critical region in 18p11.3
OVERHAUSER, J, MITCHELL, H. F, ZACKAI, E. H, TICK, D. B, ROJAS, K, MUENKE, M
Published in American journal of human genetics (01.11.1995)
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Published in American journal of human genetics (01.11.1995)
Journal Article
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome
MUENKE, M, BONE, L. J, TESSIER-LAVIGNE, M, PATTERSON, D, MITCHELL, H. F, HART, I, WALTON, K, HALL-JOHNSON, K, IPPEL, E. F, DIETZ-BAND, J, KVALØY, K, CHEN-MING FAN
Published in American journal of human genetics (01.11.1995)
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Published in American journal of human genetics (01.11.1995)
Journal Article
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2
Robin, Nathaniel H, Feldman, George J, Aronson, Adam L, Mitchell, Heather F, Weksberg, Rosanna, Leonard, Claire O, Burton, Barbara K, Josephson, Kevin D, Laxová, Renata, Aleck, Kyrieckos A, Allanson, Judith E, Guion-Almeida, Maria Leine, Martin, Rick A, Leichtman, Lawrence G, Price, R. Arlen, Opitz, John M, Muenke, Maximilian
Published in Nature genetics (01.12.1995)
Published in Nature genetics (01.12.1995)
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Journal Article
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneity
Robin, N H, Feldman, G J, Mitchell, H F, Lorenz, P, Wilroy, R S, Zackai, E H, Allanson, J E, Reich, E W, Pfeiffer, R A, Clarke, L A
Published in Human molecular genetics (01.12.1994)
Published in Human molecular genetics (01.12.1994)
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