Mapping Recombination Hotspots in Human Phosphoglucomutase (PGM1) von Ping Yip, Shea, Lovegrove, Jenny U., Rana, Naheed A., Hopkinson, David A., Whitehouse, David B.

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A phylogenetic approach to the identification of phosphoglucomutase genes von Whitehouse, D B, Tomkins, J, Lovegrove, J U, Hopkinson, D A, McMillan, W O

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The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27 von Edwards, Y H, Putt, W, Lekoape, K M, Stott, D, Fox, M, Hopkinson, D A, Sowden, J

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An interferometric test of time reversal invariance in atoms von Hopkinson, D A, Baird, P E G

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Improvement of SSCP Analysis by Use of Denaturants von Yip, Shea Ping, Hopkinson, David A, Whitehouse, David B

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Detection of ABO blood group polymorphism by denaturing gradient gel electrophoresis von Johnson, P. H., Hopkinson, D. A.

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The canine homeobox gene MSX2: sequence, chromosome assignment and genetic analysis in dogs of different breeds von Haworth, K., Breen, M., Binns, M., Hopkinson, D. A., Edwards, Y. H.

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The long [E/e] and the short [C/c] of the rhesus polymorphism von Hopkinson, David A

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Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1) von YIP, S. P., PUTT, W., HOPKINSON, D. A., WHITEHOUSE, D. B.

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The Classical Human Phosphoglucomutase (PGM1) Isozyme Polymorphism is Generated by Intragenic Recombination von March, R. E., Putt, W., Hollyoake, M., Ives, J. H., Lovegrove, J. U., Hopkinson, D. A., Edwards, Y. H., Whitehouse, D. B.

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Molecular and cytological investigations of phosphoglucomutase (PGM1) in the K562 cell line von TOMKINS, J., FOX, M., LOVEGROVE, J. U., PARRINGTON, J., HOPKINSON, D. A., WHITEHOUSE, D. B.

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DFB laser diode operation at 77 K von Hopkinson, D A, Cornish, S L, Edwards, N H, Baird, P E G, Cockburn, A, Cameron, K

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Efficient strategy for the detection of mutations in acrogeric Ehlers-danlos syndrome type IV von Johnson, P. H., Richards, A. J., Lloyd, J. C., Pope, F. M., Hopkinson, D. A.

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Inosine triphosphate pyrophosphohydrolase deficiency in a kindred with adenosine deaminase deficiency von Duley, John A., Simmonds, H.Anne, Hopkinson, David A., Levinsky, Roland J.

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A COL3A1 glycine 1006 to glutamic acid substitution in a patient with ehlers‐danlos syndrome type IV detected by denaturing gradient gel electrophoresis von Johnson, P. H., Richards, A. J., Pope, F. M., Hopkinson, D. A.

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Variation in alpha-1-antitrypsin phenotypes associated with penicillamine therapy von Whitehouse, David B., Lovegrove, Jenny U., Hopkinson, David A.

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Phosphoglucomutase 1: Complete Human and Rabbit mRNA Sequences and Direct Mapping of this Highly Polymorphic Marker on Human Chromosome 1 von Whitehouse, D. B., Putt, W., Lovegrove, J. U., Morrison, K., Hollyoake, M., Fox, M. F., Hopkinson, D. A., Edwards, Y. H.

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Human FAD-dependent NAD(P)H diaphorase von Edwards, Y H, Potter, J, Hopkinson, D A

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Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: A study of 17 cases von Abbott, C. M., Lovegrove, J. U., Whitehouse, D. B., Hopkinson, D. A., Povey, S.

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ABO genotyping of complete hydatidiform moles von FISHER, R. A, JOHNSON, P. H, POVEY, S, HOPKINSON, D. A, LAWLER, S. D

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