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Ochs, HD
Furga, AS
Valiaho, J
van Hove, JLK
Vihinen, M
Vujic, D
Vezzoni, P
Villa, A
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Citation: Jm. Johnson et al., First-trimester increased nuchal translucency and fetal hypokinesia associated with Zellweger syndrome, ULTRASOUN O, 17(4), 2001, pp. 344-346
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Authors:
Gong, YQ
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Citation: Yq. Gong et al., Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis, NAT GENET, 21(3), 1999, pp. 302-304
Authors:
Allingham-Hawkins, SJ
Babul-Hirji, R
Chitayat, D
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Citation: Sj. Allingham-hawkins et al., Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data, AM J MED G, 83(4), 1999, pp. 322-325
Authors:
Gong, YQ
Chitayat, D
Kerr, B
Chen, TP
Babul-Hirji, R
Pal, A
Reiss, M
Warman, ML
Citation: Yq. Gong et al., Brachydactyly type B: Clinical description, genetic mapping to chromosome 9q, and evidence for a shaved ancestral mutation, AM J HU GEN, 64(2), 1999, pp. 570-577