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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
Euchromatic 9q + heteromorphism in a family.
Jalal SM, Kukolich MK, Garcia M, Day DW. Jalal SM, et al. Am J Med Genet. 1990 Sep;37(1):155-6. doi: 10.1002/ajmg.1320370135. Am J Med Genet. 1990. PMID: 2240035 No abstract available.
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
Rare 15q duplication in an abortus.
Jalal SM, Day DW, Nelson MC. Jalal SM, et al. Am J Med Genet. 1989 Jul;33(3):422-3. doi: 10.1002/ajmg.1320330328. Am J Med Genet. 1989. PMID: 2801780 No abstract available.
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