Torthaí cuardaigh - Callen, D F

Alternative interpretation of reported paracentric inversion. de réir Callen, D F

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A rare heteromorphism of chromosome 20 and reproductive loss. de réir Romain, D R, Whyte, S, Callen, D F, Eyre, H J

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Anonymous DNA probes to human chromosome 16 derived from a flow-purified library. de réir Hyland, V J, Grist, S, Callen, D F, Sutherland, G R

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Necropsy findings in a fetus with a 46,XY,dic t(X;21)(p11.1;p11.1). de réir Smith, N M, Fernandez, H, Chambers, H M, Callen, D F

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Simultaneous trisomy 9q3 and monosomy 5p in two children with der(5),t(5;9)(p15.1;q34.13): report of an extended family. de réir Wellesley, D, Young, I D, Cooke, P, Callen, D F, Hockey, A

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ACHF249 [D22S14] detects a common PstI RFLP and maps at 22cen----22q13.1. de réir Fratini, A, Baker, E G, Callen, D F, Hyland, V J, Sutherland, G R

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RsaI and TaqI RFLPs for pACHF3.5 [D16S10]. de réir Fratini, A, Baker, E G, Callen, D F, Hyland, V J, Sutherland, G R

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Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16. de réir Callen, D F, Ringenbergs, M L, Fowler, J C, Freemantle, C J, Haan, E A

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Molecular genetics of human chromosome 16. de réir Sutherland, G R, Reeders, S, Hyland, V J, Callen, D F, Fratini, A, Mulley, J C

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Mapping the human alpha globin gene complex to 16p13.2----pter. de réir Simmers, R N, Mulley, J C, Hyland, V J, Callen, D F, Sutherland, G R

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pACHF1.1 [D16S8] detects a common PvuII RFLP and maps at 16p13.3----16p13.11. de réir Fratini, A, Baker, E G, Callen, D F, Reeders, S, Hyland, V J, Sutherland, G R

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Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics. de réir Callen, D F, Eyre, H J, Ringenbergs, M L, Freemantle, C J, Woodroffe, P, Haan, E A

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Dinucleotide repeat polymorphism at the D16S288 locus de réir Shen, Y., Holman, K., Thompson, A., Kozman, H., Callen, D.F., Sutherland, G.R., Richards, R.I.

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Dinucleotide repeat polymorphism at D16S287 de réir Phillips, H.A., Hyland, V.J., Holman, K., Callen, D.F., Richards, R.I., Mulley, J.C.

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TaqI RFLP identified by probe VK17A (DXS294) at Xq26. de réir Suthers, G K, Hyland, V J, Baker, E, Fernandez, K E, Callen, D F, Sutherland, G R

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The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization. de réir Callen, D F, Freemantle, C J, Ringenbergs, M L, Baker, E, Eyre, H J, Romain, D, Haan, E A

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Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4. de réir Fang, Y Y, Eyre, H J, Bohlander, S K, Estop, A, McPherson, E, Träger, T, Riess, O, Callen, D F

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An STS at the D16S290 locus. de réir Chen, L Z, Shen, Y, Holman, K, Thompson, A, Lane, S, Richards, R I, Sutherland, G R, Callen, D F

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Incidence and origin of "null" alleles in the (AC)n microsatellite markers. de réir Callen, D F, Thompson, A D, Shen, Y, Phillips, H A, Richards, R I, Mulley, J C, Sutherland, G R

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The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3. de réir Baker, E, Guo, X H, Orsborn, A M, Sutherland, G R, Callen, D F, Hopwood, J J, Morris, C P

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