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Results:
1-7
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Results: 7
Authors:
Pettenati, MJ
Berry, M
Shashi, V
Bowen, JH
Harper, M
Citation: Mj. Pettenati et al., Prenatal diagnosis of complete sole trisomy 1q, PRENAT DIAG, 21(6), 2001, pp. 435-440
Authors:
Shashi, V
Rickheim, A
Pettenati, MJ
Citation: V. Shashi et al., Maternal homozygosity for the common MTHFR mutation as a potential risk factor for offspring with limb defects, AM J MED G, 100(1), 2001, pp. 25-29
Authors:
Shashi, V
Berry, MN
Shoaf, S
Sciote, JJ
Goldstein, D
Hart, TC
Citation: V. Shashi et al., A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27, AM J HU GEN, 66(2), 2000, pp. 469-479
Authors:
Hart, TC
Price, JA
Bobby, PL
Pettenati, MJ
Shashi, V
Herr, CV
Van Dyke, TE
Citation: Tc. Hart et al., Cytogenetic assignment and physical mapping of the human DGKE gene to chromosome 17q22, GENOMICS, 56(2), 1999, pp. 233-235
Authors:
Shashi, V
Berry, MN
Santos, C
Pettenati, MJ
Citation: V. Shashi et al., Partial duplication of 4q12q13 leads to a mild phenotype, AM J MED G, 86(1), 1999, pp. 51-53
Authors:
Shashi, V
Pallos, D
Pettenati, MJ
Cortelli, JR
Fryns, JP
von Kap-Herr, C
Hart, TC
Citation: V. Shashi et al., Genetic heterogeneity of gingival fibromatosis on chromosome 2p, J MED GENET, 36(9), 1999, pp. 683-686
Authors:
Shashi, V
Berry, D
Stamper, TH
Pettenati, M
Citation: V. Shashi et al., A further case of choanal atresia in the deletion (9p) syndrome, AM J MED G, 80(4), 1998, pp. 440-440
Risultati:
1-7
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