D. F. Callen

Characterisation of Copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3 (1999)

Savino, M., D'Apolito, Maria, Centra, M., Van Beerendonk, H. M., Whitmore, S. A., ...

Characterisation of Copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3 (1999)

Savino, M., D'Apolito, Maria, Centra, M., Van Beerendonk, H. M., Whitmore, S. A., ...

Origins of accessory small ring marker chromosomes derived from chromosome 1 (1999)

Callen, D. F., Eyre, H. J., Veleba, A., Martin, N. J., ...

Three patients with accessory small ring chromosomes derived from chromosome 1 are presented together with additional clinical details and cytogenetic analyses of a previously reported patient....

Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2psi: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene (1998)

Renard, J, Doggett, N A, Callen, D F, ...

The search for the carbohydrate-deficient glycoprotein syndrome type I (CDG1) gene has revealed the existence of a family of phosphomannomutase (PMM) genes in humans. Two expressed PMM genes, PMM1...

Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13. (1998)

Nomiyama, H., Imai, Tomoya, Kusuda, J., Miura, R., Callen, D. F., Yoshie, O.

Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13. (1998)

Nomiyama, H., Imai, Tomoya, Kusuda, J., Miura, R., Callen, D. F., Yoshie, O.

Construction of an ~700-kb transcript map around the Familial Mediterranean Fever locus on human chromosome 16p13.3 (1998)

Centola, M., Chen, X., Sood, R., Deng, Z., Aksentijevich, I., Blake, T., ...

High resolution characterisation of an interstitial deletion of less than 1.9Mb at 4p16.3 associated with Wolf-Hirschhorn Syndrome (1997)

Fang, Y. Y., Bain, S., Haan, E. A., Eyre, H. J., MacDonald, M., Wright, T. J., ...

Assignment of the Human CC Chemokine Gene TARC (SCYA17) to chromosome 16q13 (1997)

Nomiyama, H., Imai, Tomoya, Kusuda, J., Miura, R., Callen, D. F., Yoshie, O.

High resolution characterisation of an interstitial deletion of less than 1.9Mb at 4p16.3 associated with Wolf-Hirschhorn Syndrome (1997)

Fang, Y. Y., Bain, S., Haan, E. A., Eyre, H. J., MacDonald, M., Wright, T. J., ...

Assignment of the Human CC Chemokine Gene TARC (SCYA17) to chromosome 16q13 (1997)

Nomiyama, H., Imai, Tomoya, Kusuda, J., Miura, R., Callen, D. F., Yoshie, O.

Positional cloning of the Fanconi anaemia group A gene (1996)

Apostolou, S., Whitmore, S A., Crawford, J., Lennon, G., Sutherland, G R., Callen, D F., ...

Positional cloning of the Fanconi anaemia group A gene (1996)

Apostolou, S., Whitmore, S A., Crawford, J., Lennon, G., Sutherland, G R., Callen, D F., ...

An integrated physical map of human chromosome 16 (1995)

Doggett, N. A., Goodwin, L. A., Tesmer, J. G., Meincke, L. J., Bruce, D. C., Clark, L. M., ...

We describe an integrated physical, genetic and cytogenetic map of human chromosome 16 comprising both a low-resolution megaYAC map and a high-resolution cosmid contig/mlnlYAC map, which provides...

An integrated physical map of human chromosome 16 (1995)

Doggett, N. A., Goodwin, L. A., Tesmer, J. G., Meincke, L. J., Bruce, D. C., Clark, L. M., ...

We describe an integrated physical, genetic and cytogenetic map of human chromosome 16 comprising both a low-resolution megaYAC map and a high-resolution cosmid contig/mlnlYAC map, which provides...

Microsatellite repeat polymorphism at the D16S366 locus (1994)

Schultz, E.A., Callen, D.F., Doggett, N.A., Haines, J.L., Lerner, T.J.

Dinucleotide repeat polumorphisms at the D16S525, D16S359. D16S531 and D16S522 loci (1994)

Shen, Y., Holman, K., Doggett, N.A., Callen, D.F., Sutherland, G.R., Richards, R.I.

Dinucleotide repeat polymorphism at D16S533 (1994)

Cleton–Jansen, A.M., Moerland, H.W., Callen, D.F., Breuning, M.H., Devilee, P.

Five dinucleotide repeat polymorphisms on human chromosome 16q24.2 - q24.3 (1993)

Shen, Y., Holman, K., Doggett, N.A., Callen, D.F., Sutherland, G.R., Richards, R.I.

Six dinucleotide repeat polymorphisms on human chromosome 16q12.1 - q24.1 (1993)

Shen, Y., Holman, K., Doggett, N.A., Callen, D.F., Sutherland, G.R., Richards, R.I.

Three dinucleotide repeat polymorphisms on human chromosome 16p 13.11-p13.3 (1993)

Shen, Y., Holman, K., Doggett, N.A., Callen, D.F., Sutherland, G.R., Richards, R.I.

Four dinucleotide repeat polymorphisms on human chromosome 16 (1993)

Shen, Y., Holman, K., Doggett, N.A., Callen, D. F., Sutherland, G.R., Richards, R.I.

Four dinucleotide repeat polymorphisms on human chromosome 16 at D16S289, D16S318, D16S319 and D1 6S320 (1992)

Shen, Y., Thompson, A.T., Holman, K., Callen, D.F., Sutherland, G.R., Richards, R.I.

Dinucleotide repeat polymorphism at the D16S288 locus (1991)

Shen, Y., Holman, K., Thompson, A., Kozman, H., Callen, D.F., Sutherland, G.R., ...

Dinucleotide repeat polymorphism at D16S287 (1991)

Phillips, H.A., Hyland, V.J., Holman, K., Callen, D.F., Richards, R.I., Mulley, J.C.

TaqI RFLP Identified by probe VK17A (DXS294) at Xq26 (1988)

Suthers, G.K., Hyland, V.J., Baker, E., Fernandez, K.E.W., Callen, D.F., Sutherland, G.R.

ACHF249 (D22S14) detects a common PstI RFLP and maps at 22cen--22q13.1 (1988)

Fratini, A., Baker, E.G., Callen, D.F., Hyland, V.J., Sutherland, G.R.

pACHF1.1 [D16S8] detects a common PvuII RFLP and maps at 16p13.3-16p13.11 (1988)

Fratini, A., Baker, E.G., Callen, D.F., Reeders, S., Hyland, V.J., Sutherland, G.R.

RsaI and TaqI RFLPs for pACHF3.5 [D16S10] (1988)

Fratini, A., Baker, E.G., Callen, D.F., Hyland, V.J., Sutherland, G.R.

Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3

Cleton-Jansen, A-M, Moerland, E W, Pronk, J C, Apostolou, S, Crawford, J, ...

The recently identified Fanconi anaemia A (FAA) gene is located on chromosomal band 16q24.3 within a region that has been frequently reported to show loss of heterozygosity (LOH) in breast cancer....