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Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16.
Lindor NM, Jalal SM, Thibodeau SN, Bonde D, Sauser KL, Karnes PS. Lindor NM, et al. Among authors: jalal sm. Clin Genet. 1993 Oct;44(4):185-9. doi: 10.1111/j.1399-0004.1993.tb03876.x. Clin Genet. 1993. PMID: 8261647
Unbalanced cryptic 5p deletion/17p duplication identified by subtelomeric FISH in a family with a boy with chimerism and a balanced t(4;5).
Ensenauer R, Jalal S, Meyer R, Babovic-Vuksanovic D. Ensenauer R, et al. Among authors: jalal s. Am J Med Genet A. 2004 Feb 15;125A(1):86-91. doi: 10.1002/ajmg.a.20420. Am J Med Genet A. 2004. PMID: 14755472
Partial 6p trisomy associated with infantile autism.
Burd L, Martsolf JT, Kerbeshian J, Jalal SM. Burd L, et al. Among authors: jalal sm. Clin Genet. 1988 May;33(5):356-9. doi: 10.1111/j.1399-0004.1988.tb03462.x. Clin Genet. 1988. PMID: 3378366
Ring chromosome 8 syndrome: further characterization.
Tonk VS, Kukolich MK, Morgan D, Khan A, Jalal SM. Tonk VS, et al. Among authors: jalal sm. Am J Med Genet. 2000 Jan 17;90(2):162-4. doi: 10.1002/(sici)1096-8628(20000117)90:2<162::aid-ajmg14>3.0.co;2-#. Am J Med Genet. 2000. PMID: 10607957
Inverted duplication involving alpha satellite DNA resulting in a C-negative-band in the qh region of chromosome 16.
Jalal SM, Law ME, Dewald GW. Jalal SM, et al. Am J Med Genet. 1993 May 15;46(3):351-2. doi: 10.1002/ajmg.1320460326. Am J Med Genet. 1993. PMID: 8488887 No abstract available.
Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) mat.
Martsolf JT, Chase TR, Jalal SM, Wasdahl WA. Martsolf JT, et al. Among authors: jalal sm. Clin Genet. 1987 Jun;31(6):366-9. doi: 10.1111/j.1399-0004.1987.tb02825.x. Clin Genet. 1987. PMID: 3621637
Two rare cases of 6p partial deletion.
Jalal SM, Macias VR, Roop H, Morgan F, King P. Jalal SM, et al. Clin Genet. 1989 Sep;36(3):196-9. doi: 10.1111/j.1399-0004.1989.tb03188.x. Clin Genet. 1989. PMID: 2477178
Trisomy 22: no longer an enigma.
Kukolich MK, Kulharya A, Jalal SM, Drummond-Borg M. Kukolich MK, et al. Among authors: jalal sm. Am J Med Genet. 1989 Dec;34(4):541-4. doi: 10.1002/ajmg.1320340417. Am J Med Genet. 1989. PMID: 2624265
Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy.
Jalal SM, Lindor NM, Michels VV, Buckley DD, Hoppe DA, Sarkar G, Dewald GW. Jalal SM, et al. Am J Med Genet. 1993 Jun 1;46(4):441-3. doi: 10.1002/ajmg.1320460419. Am J Med Genet. 1993. PMID: 8357018
Familial transmission of 16p trisomy in an infant.
Jalal SM, Day DW, Garcia M, Benjamin T, Rogers J. Jalal SM, et al. Hum Genet. 1989 Jan;81(2):196-8. doi: 10.1007/BF00293904. Hum Genet. 1989. PMID: 2912890
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