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Results: 1-17 |
Results: 17
Voltage-gated calcium channel gamma 2 subunit gene is not deleted in velo-cardio-facial syndrome
Authors: Black, JL Krahn, LE Jalal, SM
Citation: Jl. Black et al., Voltage-gated calcium channel gamma 2 subunit gene is not deleted in velo-cardio-facial syndrome, MOL PSYCHI, 6(4), 2001, pp. 461-464
Tandem translocation of chromosomes 22 and 15 with two preserved satellitestalk regions and deletion 22q13.3-qter
Authors: Lee, KA Kim, SH Lee, MH Law, ME Jalal, SM
Citation: Ka. Lee et al., Tandem translocation of chromosomes 22 and 15 with two preserved satellitestalk regions and deletion 22q13.3-qter, AM J MED G, 104(4), 2001, pp. 291-294
Analysis of hurthle cell neoplasms of the thyroid by interphase fluorescence in situ hybridization
Authors: Erickson, LA Jalal, SM Goellner, JR Law, ME Harwood, A Jin, L Roche, PC Lloyd, RV
Citation: La. Erickson et al., Analysis of hurthle cell neoplasms of the thyroid by interphase fluorescence in situ hybridization, AM J SURG P, 25(7), 2001, pp. 911-917
Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disorders
Authors: Jalal, SM Law, ME Lindor, NM Thompson, KJ Sekhon, GS
Citation: Sm. Jalal et al., Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disorders, MAYO CLIN P, 76(1), 2001, pp. 16-21
Detection of diagnostically critical, often hidden, anomalies in complex karyotypes of haematological disorders using multicolour fluorescence in situ hybridization
Authors: Jalal, SM Law, ME Stamberg, J Fonseca, R Seely, JR Myers, WH Hanson, CA
Citation: Sm. Jalal et al., Detection of diagnostically critical, often hidden, anomalies in complex karyotypes of haematological disorders using multicolour fluorescence in situ hybridization, BR J HAEM, 112(4), 2001, pp. 975-980
Translocations involving the immunoglobulin heavy-chain locus are possibleearly genetic events in patients with primary systemic amyloidosis
Authors: Hayman, SR Bailey, RJ Jalal, SM Ahmann, GJ Dispenzieri, A Gertz, MA Greipp, PR Kyle, RA Lacy, MQ Rajkumar, SV Witzig, TE Lust, JA Fonseca, R
Citation: Sr. Hayman et al., Translocations involving the immunoglobulin heavy-chain locus are possibleearly genetic events in patients with primary systemic amyloidosis, BLOOD, 98(7), 2001, pp. 2266-2268
Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin
Authors: Mao, R Jalal, SM Snow, K Michels, VV Szabo, SM Babovic-Vuksanovic, D
Citation: R. Mao et al., Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin, GENET MED, 2(2), 2000, pp. 131-135
Pulmonary lymphangioleiomyomatosis in a man
Authors: Aubry, MC Myers, JL Ryu, JH Henske, EP Logginidou, H Jalal, SM Tazelaar, HD
Citation: Mc. Aubry et al., Pulmonary lymphangioleiomyomatosis in a man, AM J R CRIT, 162(2), 2000, pp. 749-752
FISH demonstrates treatment-related chromosome damage in myeloid but not plasma cells in primary systemic amyloidosis
Authors: Fonseca, R Rajkumar, SV Ahmann, GJ Jalal, SM Hoyer, JD Gertz, MA Kyle, RA Greipp, PR Dewald, GW
Citation: R. Fonseca et al., FISH demonstrates treatment-related chromosome damage in myeloid but not plasma cells in primary systemic amyloidosis, LEUK LYMPH, 39(3-4), 2000, pp. 391
Inherited interstitial deletion of chromosomes 5p and 16q without apparentphenotypic effect: further confirmation
Authors: Hand, JL Michels, VV Marinello, MJ Ketterling, RP Jalal, SM
Citation: Jl. Hand et al., Inherited interstitial deletion of chromosomes 5p and 16q without apparentphenotypic effect: further confirmation, PRENAT DIAG, 20(2), 2000, pp. 144-148
Ring chromosome 8 syndrome: Further characterization
Authors: Tonk, VS Kukolich, MK Morgan, D Khan, A Jalal, SM
Citation: Vs. Tonk et al., Ring chromosome 8 syndrome: Further characterization, AM J MED G, 90(2), 2000, pp. 162-164
Utility of multicolor fluorescent in situ hybridization in clinical cytogenetics
Authors: Jalal, SM Law, ME
Citation: Sm. Jalal et Me. Law, Utility of multicolor fluorescent in situ hybridization in clinical cytogenetics, GENET MED, 1(5), 1999, pp. 181-186
Clinical significance of the translocation (11;14)(q13;q32) in multiple myeloma
Authors: Fonseca, R Hoyer, JD Aguayo, P Jalal, SM Ahmann, GJ Rajkumar, SV Witzig, TE Lacy, MQ Dispenzieri, A Gertz, MA Kyle, RA Greipp, PR
Citation: R. Fonseca et al., Clinical significance of the translocation (11;14)(q13;q32) in multiple myeloma, LEUK LYMPH, 35(5-6), 1999, pp. 599-605
Guidelines for buccal smear collection in breast-fed infants
Authors: Babovic-Vuksanovic, D Michels, VV Law, ME Bailey, R Wyatt, WA Lindor, NM Jalal, SM
Citation: D. Babovic-vuksanovic et al., Guidelines for buccal smear collection in breast-fed infants, AM J MED G, 84(4), 1999, pp. 357-360
Detection of t(2;5) in anaplastic large cell lymphoma - Comparison of immunohistochemical studies, FISH, and RT-PCR in paraffin-embedded tissue
Authors: Cataldo, KA Jalal, SM Law, ME Ansell, SM Inwards, DJ Fine, M Arber, DA Pulford, KA Strickler, JG
Citation: Ka. Cataldo et al., Detection of t(2;5) in anaplastic large cell lymphoma - Comparison of immunohistochemical studies, FISH, and RT-PCR in paraffin-embedded tissue, AM J SURG P, 23(11), 1999, pp. 1386-1392
Visual impairment due to macular disciform scars in a 20-year-old man withSmith-Magenis syndrome: Another ophthalmologic complication
Authors: Babovic-Vuksanovic, D Jalal, SM Garrity, JA Robertson, DM Lindor, NM
Citation: D. Babovic-vuksanovic et al., Visual impairment due to macular disciform scars in a 20-year-old man withSmith-Magenis syndrome: Another ophthalmologic complication, AM J MED G, 80(4), 1998, pp. 373-376
Chromosomal abnormalities in systemic amyloidosis
Authors: Fonseca, R Ahmann, GJ Jalal, SM Dewald, GW Larson, DR Therneau, TM Gertz, MA Kyle, RA Greipp, PR
Citation: R. Fonseca et al., Chromosomal abnormalities in systemic amyloidosis, BR J HAEM, 103(3), 1998, pp. 704-710
Risultati: 1-17 |