Ivens AC - Search Results

1

The generation of ordered sets of cosmid DNA clones from human chromosome region 11p.

Heding IJ, Ivens AC, Wilson J, Strivens M, Gregory S, Hoovers JM, Mannens M, Redeker B, Porteous D, van Heyningen V, et al. Heding IJ, et al. Among authors: ivens ac. Genomics. 1992 May;13(1):89-94. doi: 10.1016/0888-7543(92)90206-8. Genomics. 1992. PMID: 1577496

2

An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.

Redeker E, Hoovers JM, Alders M, van Moorsel CJ, Ivens AC, Gregory S, Kalikin L, Bliek J, de Galan L, van den Bogaard R, et al. Redeker E, et al. Among authors: ivens ac. Genomics. 1994 Jun;21(3):538-50. doi: 10.1006/geno.1994.1312. Genomics. 1994. PMID: 7959730 Free article.

3

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

Hoovers JM, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillon-Miller P, Schlessinger D, Edwards MC, Elledge SJ, Ivens A, Westerveld A, Little P, Mannens M, Feinberg AP. Hoovers JM, et al. Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12456-60. doi: 10.1073/pnas.92.26.12456. Proc Natl Acad Sci U S A. 1995. PMID: 8618920 Free PMC article.

4

Structure and sequence of the human homeobox gene HOX7.

Hewitt JE, Clark LN, Ivens A, Williamson R. Hewitt JE, et al. Genomics. 1991 Nov;11(3):670-8. doi: 10.1016/0888-7543(91)90074-o. Genomics. 1991. PMID: 1685479

5

The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome.

Ivens A, Flavin N, Williamson R, Dixon M, Bates G, Buckingham M, Robert B. Ivens A, et al. Hum Genet. 1990 Apr;84(5):473-6. doi: 10.1007/BF00195823. Hum Genet. 1990. PMID: 1969845

6

11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.

Puech A, Ahnine L, Lüdecke HJ, Senger G, Ivens A, Jeanpierre C, Little P, Horsthemke B, Claussen U, Jones C, et al. Puech A, et al. Genomics. 1992 Aug;13(4):1274-80. doi: 10.1016/0888-7543(92)90046-u. Genomics. 1992. PMID: 1380484

7

The application of molecular genetics to detection of craniofacial abnormality.

Moore G, Ivens A, Chambers J, Bjornsson A, Arnason A, Jensson O, Williamson R. Moore G, et al. Development. 1988;103 Suppl:233-9. doi: 10.1242/dev.103.Supplement.233. Development. 1988. PMID: 3074911

8

Genomics and the biology of parasites.

Johnston DA, Blaxter ML, Degrave WM, Foster J, Ivens AC, Melville SE. Johnston DA, et al. Among authors: ivens ac. Bioessays. 1999 Feb;21(2):131-47. doi: 10.1002/(SICI)1521-1878(199902)21:2<131::AID-BIES7>3.0.CO;2-I. Bioessays. 1999. PMID: 10193187 Review.

9

Gene copy number variation throughout the Plasmodium falciparum genome.

Cheeseman IH, Gomez-Escobar N, Carret CK, Ivens A, Stewart LB, Tetteh KK, Conway DJ. Cheeseman IH, et al. BMC Genomics. 2009 Aug 4;10:353. doi: 10.1186/1471-2164-10-353. BMC Genomics. 2009. PMID: 19653891 Free PMC article.

10

X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17.

Ivens A, Moore GE, Chambers J, Arnason A, Jensson O, Bjornsson A, Williamson R. Ivens A, et al. Hum Genet. 1988 Apr;78(4):356-8. doi: 10.1007/BF00291735. Hum Genet. 1988. PMID: 2896158

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