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Results:
1-7
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Results: 7
Prenatal diagnosis of complete sole trisomy 1q
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
Maternal homozygosity for the common MTHFR mutation as a potential risk factor for offspring with limb defects
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
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27
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
Cytogenetic assignment and physical mapping of the human DGKE gene to chromosome 17q22
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
Partial duplication of 4q12q13 leads to a mild phenotype
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
Genetic heterogeneity of gingival fibromatosis on chromosome 2p
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
A further case of choanal atresia in the deletion (9p) syndrome
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:
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