Haddad L - Search Results

1

Simplified detection of a mutation causing familial hypercholesterolaemia throughout Britain: evidence for an origin in a common distant ancestor.

Wenham PR, Haddad L, Panarelli M, Ashby JP, Day IN, Giles PD, Humphries SE, Penney MD, Rae PW, Walker SW. Wenham PR, et al. Among authors: haddad l. Ann Clin Biochem. 1998 Mar;35 ( Pt 2):226-35. doi: 10.1177/000456329803500205. Ann Clin Biochem. 1998. PMID: 9547893

2

Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of Scotland.

Lee WK, Haddad L, Macleod MJ, Dorrance AM, Wilson DJ, Gaffney D, Dominiczak MH, Packard CJ, Day IN, Humphries SE, Dominiczak AF. Lee WK, et al. Among authors: haddad l. J Med Genet. 1998 Jul;35(7):573-8. doi: 10.1136/jmg.35.7.573. J Med Genet. 1998. PMID: 9678702 Free PMC article.

3

High-throughput method for determination of apolipoprotein E genotypes with use of restriction digestion analysis by microplate array diagonal gel electrophoresis.

Bolla MK, Haddad L, Humphries SE, Winder AF, Day IN. Bolla MK, et al. Among authors: haddad l. Clin Chem. 1995 Nov;41(11):1599-604. Clin Chem. 1995. PMID: 7586549

4

Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394.

Day IN, Haddad L, O'Dell SD, Day LB, Whittall RA, Humphries SE. Day IN, et al. Among authors: haddad l. J Med Genet. 1997 Feb;34(2):111-6. doi: 10.1136/jmg.34.2.111. J Med Genet. 1997. PMID: 9039985 Free PMC article.

5

Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia.

Day IN, Whittall RA, O'Dell SD, Haddad L, Bolla MK, Gudnason V, Humphries SE. Day IN, et al. Among authors: haddad l. Hum Mutat. 1997;10(2):116-27. doi: 10.1002/(SICI)1098-1004(1997)10:2<116::AID-HUMU4>3.0.CO;2-I. Hum Mutat. 1997. PMID: 9259195

6

Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindreds.

Haddad L, Day LB, Attwood J, Povey S, Humphries SE, Day IN. Haddad L, et al. Ann Hum Genet. 1997 Nov;61(Pt 6):497-506. doi: 10.1046/j.1469-1809.1997.6160497.x. Ann Hum Genet. 1997. PMID: 9543550

7

Applicability of LDLR flanking microsatellite polymorphisms for prenatal diagnosis of homozygous state for familial hypercholesterolemia.

De Oliveira e Silva ER, Haddad L, Kwiterovich PO Jr, Humphries SE, Day IN. De Oliveira e Silva ER, et al. Among authors: haddad l. Clin Genet. 1998 May;53(5):375-8. doi: 10.1111/j.1399-0004.1998.tb02748.x. Clin Genet. 1998. PMID: 9660055

8

Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindred.

Haddad L, Day IN, Hunt S, Williams RR, Humphries SE, Hopkins PN. Haddad L, et al. J Lipid Res. 1999 Jun;40(6):1113-22. J Lipid Res. 1999. PMID: 10357843 Free article.

9

A World Wide Web site for low-density lipoprotein receptor gene mutations in familial hypercholesterolemia: sequence-based, tabular, and direct submission data handling.

Wilson DJ, Gahan M, Haddad L, Heath K, Whittall RA, Williams RR, Humphries SE, Day IN. Wilson DJ, et al. Among authors: haddad l. Am J Cardiol. 1998 Jun 15;81(12):1509-11. doi: 10.1016/s0002-9149(98)00215-x. Am J Cardiol. 1998. PMID: 9645910

10

Microtiter Array Diagonal Gel Electrophoresis (MADGE) for Population Scale Genotype Analyses.

Day IN, Bolla M, Haddad L, O'Dell S, Humphries SE. Day IN, et al. Among authors: haddad l. Methods Mol Med. 1996;5:269-81. doi: 10.1385/0-89603-346-5:269. Methods Mol Med. 1996. PMID: 21374524

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