Ngā hua rapu kaituhi

1

Alternative interpretation of reported paracentric inversion. mā Callen, D F

I whakaputaina 1998

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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2

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

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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3

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

I whakaputaina 1988

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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4

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

I whakaputaina 1992

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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5

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

I whakaputaina 1988

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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6

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

I whakaputaina 1988

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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7

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

I whakaputaina 1988

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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8

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

I whakaputaina 1990

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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9

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

I whakaputaina 1987

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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10

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

I whakaputaina 1987

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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11

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

I whakaputaina 1988

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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12

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

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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13

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

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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14

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

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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15

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

I whakaputaina 1988

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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16

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

I whakaputaina 1990

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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17

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

I whakaputaina 1995

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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18

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

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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19

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

I whakaputaina 1993

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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20

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

I whakaputaina 1993

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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Ngā hua rapu - Callen, D F

Alternative interpretation of reported paracentric inversion. mā Callen, D F

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

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

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

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

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

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

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

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

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

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

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

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

Dinucleotide repeat polymorphism at D16S287 mā 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. mā Suthers, G K, Hyland, V J, Baker, E, Fernandez, K E, Callen, D F, Sutherland, G R

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

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

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

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

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

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