Syed M Jalal
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Explore the profile of Syed M Jalal including associated specialties, affiliations and a list of published articles.
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28
Citations
468
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Recent Articles
1.
Shearer B, Thorland E, Carlson A, Jalal S, Ketterling R
Genet Med
. 2011 Mar;
13(6):545-52.
PMID: 21415758
Introduction: The use of chromosome analysis on products of conception from spontaneous abortions is recommended to identify a genetic etiology. However, 20% of products of conception cultures are unsuccessful due...
2.
Mitchell E, Leonhard K, Stupca P, Jalal S, Lindor N
J Assoc Genet Technol
. 2008 Mar;
34(1):5-7.
PMID: 18322350
Abnormal gene dosage usually results in recognizable phenotypic abnormalities, especially if it involves a series of contiguous genes. Schmickel (1986) defined contiguous gene syndromes as diseases resulting from loss or...
3.
Merritt 2nd J, Zou Y, Jalal S, Michels V
Am J Med Genet A
. 2007 Feb;
143A(6):599-603.
PMID: 17304549
The 1qter microdeletion is often reported in the literature as a part of a complex chromosome rearrangement. We describe a patient with a normal initial cytogenetic analysis later found by...
4.
Lindor N, Jalal S, Kumar S, Lteif A
Am J Med Genet A
. 2006 Nov;
143A(1):95-7.
PMID: 17103457
No abstract available.
5.
Mandal D, Srivastava A, Mahlum E, Desai D, Maran A, Yaszemski M, et al.
Gene
. 2006 Nov;
386(1-2):131-8.
PMID: 17079093
Deciphering the molecular basis of cancer is critical for developing novel diagnostic and therapeutic strategies. To better understand the early molecular events involving osteogenic sarcoma (OGS), we have initiated a...
6.
Zou Y, Van Dyke D, Thorland E, Chhabra H, Michels V, Keefe J, et al.
Am J Med Genet A
. 2006 Jul;
140(15):1696-706.
PMID: 16835934
Ring chromosome 20 is a rare chromosome disorder characterized by a typical seizure phenotype consisting of complex partial seizures, frequent progression to generalized tonic or tonic-clonic seizures, and nocturnal frontal...
7.
Finch R, Moore H, Lindor N, Jalal S, Markowitz A, Suresh J, et al.
Dis Colon Rectum
. 2005 Oct;
48(11):2148-52.
PMID: 16228830
Familial adenomatous polyposis, caused by mutations in the adenomatous polyposis coli gene located at chromosome 5q21, is an autosomal dominant syndrome characterized by polyposis of the colon and rectum and...
8.
Chng W, Van Wier S, Ahmann G, Winkler J, Jalal S, Bergsagel P, et al.
Blood
. 2005 May;
106(6):2156-61.
PMID: 15920009
Two major genetic categories of multiple myeloma (MM) exist. Hyperdiploid MM (48 to 74 chromosomes, median 53 chromosomes) is associated with trisomies especially of chromosomes 3, 7, 9, 11, 15,...
9.
Adeyinka A, Adams S, Lorentz C, Van Dyke D, Jalal S
Am J Med Genet A
. 2005 Apr;
135(1):28-35.
PMID: 15810004
In recent years, strategies have been developed to investigate the possible role of chromosomal subtelomere regions in genetic disorders. The present study was to determine the incidence of familial subtelomeric...
10.
Velagaleti G, Bien-Willner G, Northup J, Lockhart L, Hawkins J, Jalal S, et al.
Am J Hum Genet
. 2005 Feb;
76(4):652-62.
PMID: 15726498
Campomelic dysplasia (CD) is a semilethal skeletal malformation syndrome with or without XY sex reversal. In addition to the multiple mutations found within the sex-determining region Y-related high-mobility group box...