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Results:
1-7
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Results: 7
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel
Authors:
Tuck-Muller, CM
Goodman, BK
Li, SB
Martinez, JE
Chen, XN
Wertelecki, W
Korenberg, JR
Stetten, G
Citation: Cm. Tuck-muller et al., Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel, GENET MED, 3(2), 2001, pp. 126-131
Authors:
Scammell, JG
Wright, JL
Tuck-Muller, CM
Citation: Jg. Scammell et al., The origin of four squirrel monkey cell lines established by karyotype analysis, CYTOG C GEN, 93(3-4), 2001, pp. 263-264
Authors:
Tuck-Muller, CM
Narayan, A
Tsien, F
Smeets, DFCM
Sawyer, J
Fiala, ES
Sohn, OS
Ehrlich, M
Citation: Cm. Tuck-muller et al., DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients (vol 89, pg 121, 2000), CYTOG C GEN, 90(3-4), 2000, pp. 329-329
Authors:
Tuck-Muller, CM
Narayan, A
Tsien, F
Smeets, DFCM
Sawyer, J
Fiala, ES
Sohn, OS
Ehrlich, M
Citation: Cm. Tuck-muller et al., DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients, CYTOG C GEN, 89(1-2), 2000, pp. 121-128
Authors:
Andersson, HC
Frentz, J
Martinez, JE
Tuck-Muller, CM
Bellizaire, J
Citation: Hc. Andersson et al., Adrenal insufficiency in Smith-Lemli-Opitz syndrome, AM J MED G, 82(5), 1999, pp. 382-384
Authors:
Martinez, JE
Tuck-Muller, CM
Gasparrini, W
Li, SB
Wertelecki, W
Citation: Je. Martinez et al., 1p microdeletion in sibs with minimal phenotypic manifestations, AM J MED G, 82(2), 1999, pp. 107-109
Authors:
Li, SB
Tuck-Muller, CM
Martinez, JE
Rowley, ER
Chen, H
Wertelecki, W
Citation: Sb. Li et al., Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH), AM J MED G, 80(5), 1998, pp. 487-490
Risultati:
1-7
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