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Results:
1-7
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Results: 7
Authors:
Eldadah, ZA
Hamosh, A
Biery, NJ
Montgomery, RA
Duke, M
Elkins, R
Dietz, HC
Citation: Za. Eldadah et al., Familial Tetralogy of Fallot caused bg mutation in the jagged1 gene (vol 10, pg 163, 2001), HUM MOL GEN, 10(9), 2001, pp. 1003-1003
Authors:
Eldadah, ZA
Hamosh, A
Biery, NJ
Montgomery, RA
Duke, M
Elkins, R
Dietz, HC
Citation: Za. Eldadah et al., Familial Tetralogy of Fallot caused by mutation in the jagged1 gene, HUM MOL GEN, 10(2), 2001, pp. 163-169
Authors:
Hamosh, A
Scott, AF
Amberger, J
Valle, D
McKusick, VA
Citation: A. Hamosh et al., Online Mendelian Inheritance in Man (OMIM), HUM MUTAT, 15(1), 2000, pp. 57-61
Authors:
Yaghmai, R
Kimyai-Asadi, A
Rostamiani, K
Heiss, NS
Poustka, A
Eyaid, W
Bodurtha, J
Nousari, HC
Hamosh, A
Metzenberg, A
Citation: R. Yaghmai et al., Overlap of dyskeratosis congenita with the Hoyeraal-Hreidarsson syndrome, J PEDIAT, 136(3), 2000, pp. 390-393
Authors:
Freeman, BM
Hoon, AH
Breiter, SN
Hamosh, A
Citation: Bm. Freeman et al., Pachygyria in Weaver syndrome, AM J MED G, 86(4), 1999, pp. 395-397
Authors:
Hamosh, A
Citation: A. Hamosh, Race, ethnicity, and genetics - Reply, J PEDIAT, 134(1), 1999, pp. 122-122
Authors:
Hofstra, RMW
Valdenaire, O
Arch, E
Osinga, J
Kroes, H
Loffler, BM
Hamosh, A
Meijers, C
Buys, CHCM
Citation: Rmw. Hofstra et al., A loss-of-function mutation in the endothelin-converting enzyme 1 (ECE-1) associated with Hirschsprung disease, cardiac defects, and autonomic dysfunction, AM J HU GEN, 64(1), 1999, pp. 304-308
Risultati:
1-7
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