Jalal S - Search Results

1

Uniparental disomy in congenital disorders: a prospective study.

Lindor NM, Karnes PS, Michels VV, Dewald GW, Goerss J, Jalal S, Jenkins RB, Vockley G, Thibodeau SN. Lindor NM, et al. Among authors: jalal s. Am J Med Genet. 1995 Aug 28;58(2):143-6. doi: 10.1002/ajmg.1320580210. Am J Med Genet. 1995. PMID: 8533805

2

Nonmosaic smallest duplication of 12q24.31-qter: the first reported case.

Ireland JW, Jalal SM, McGrann PS, Lindor NM. Ireland JW, et al. Among authors: jalal sm. Am J Med Genet A. 2004 Jul 30;128A(3):305-10. doi: 10.1002/ajmg.a.30098. Am J Med Genet A. 2004. PMID: 15216553

3

Delineation of the cryptic 1qter deletion phenotype.

Merritt JL 2nd, Zou Y, Jalal SM, Michels VV. Merritt JL 2nd, et al. Am J Med Genet A. 2007 Mar 15;143A(6):599-603. doi: 10.1002/ajmg.a.31611. Am J Med Genet A. 2007. PMID: 17304549

4

De novo 16p deletion: ATR-16 syndrome.

Lindor NM, Valdes MG, Wick M, Thibodeau SN, Jalal S. Lindor NM, et al. Among authors: jalal s. Am J Med Genet. 1997 Nov 12;72(4):451-4. Am J Med Genet. 1997. PMID: 9375730

5

Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin.

Mao R, Jalal SM, Snow K, Michels VV, Szabo SM, Babovic-Vuksanovic D. Mao R, et al. Among authors: jalal sm. Genet Med. 2000 Mar-Apr;2(2):131-5. doi: 10.1097/00125817-200003000-00003. Genet Med. 2000. PMID: 11397326 Free article. Review.

6

Cytogenetic guidelines for fragile X studies tested in routine practice.

Dewald GW, Buckley DD, Spurbeck JL, Jalal SM. Dewald GW, et al. Among authors: jalal sm. Am J Med Genet. 1992 Dec 1;44(6):816-21. doi: 10.1002/ajmg.1320440620. Am J Med Genet. 1992. PMID: 1481854 Review.

7

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

8

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

9

Method for sequential staining of GTL-banded metaphases with fluorescent-labeled chromosome-specific paint probes.

Jalal SM, Law ME, Christensen ER, Spurbeck JL, Dewald GW. Jalal SM, et al. Am J Med Genet. 1993 Apr 1;46(1):98-103. doi: 10.1002/ajmg.1320460117. Am J Med Genet. 1993. PMID: 8494038

10

Cytogenetic and clinical characteristics of a case involving complete duplication of Xpter-->Xq13.

Jalal SM, Dahl R, Erickson L, Zimmerman D, Lindor N. Jalal SM, et al. J Med Genet. 1996 Mar;33(3):237-9. doi: 10.1136/jmg.33.3.237. J Med Genet. 1996. PMID: 8728700 Free PMC article.

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