Results
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141.
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142.
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143.
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144.
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Extra embryonic/fetal karyotypic discordance during diagnostic chorionic villus sampling. [electronic resource] by
- Callen, D F
- Korban, G
- Dawson, G
- Gugasyan, L
- Krumins, E J
- Eichenbaum, S
- Petrass, J
- Purvis-Smith, S
- Smith, A
- Den Dulk, G
Producer: 19890215
In:
Prenatal diagnosis vol. 8
Availability: No items available.
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145.
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146.
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147.
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148.
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Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1). [electronic resource] by
- Scott, I C
- Halila, R
- Jenkins, J M
- Mehan, S
- Apostolou, S
- Winqvist, R
- Callen, D F
- Prockop, D J
- Peltonen, L
- Kadler, K E
Producer: 19961121
In:
Gene vol. 174
Availability: No items available.
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149.
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150.
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Reduction of the genetic interval for lyphoedema-distichiasis to below 2 Mb. [electronic resource] by
- Bell, R
- Brice, G
- Child, A H
- Murday, V A
- Mansour, S
- Sandy, C J
- Collin, J R
- Mortimer, P
- Callen, D F
- Burnand, K
Producer: 20001116
In:
Journal of medical genetics vol. 37
Availability: No items available.
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151.
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Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1. [electronic resource] by
- Klanke, C A
- Su, Y R
- Callen, D F
- Wang, Z
- Meneton, P
- Baird, N
- Kandasamy, R A
- Orlowski, J
- Otterud, B E
- Leppert, M
Producer: 19950629
In:
Genomics vol. 25
Availability: No items available.
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152.
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153.
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154.
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Characterization 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. [electronic resource] by
- Savino, M
- d'Apolito, M
- Centra, M
- van Beerendonk, H M
- Cleton-Jansen, A M
- Whitmore, S A
- Crawford, J
- Callen, D F
- Zelante, L
- Savoia, A
Producer: 19991209
In:
Genomics vol. 61
Availability: No items available.
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155.
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156.
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Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1). [electronic resource] by
- Breuning, M H
- Snijdewint, F G
- Brunner, H
- Verwest, A
- Ijdo, J W
- Saris, J J
- Dauwerse, J G
- Blonden, L
- Keith, T
- Callen, D F
Producer: 19910108
In:
Journal of medical genetics vol. 27
Availability: No items available.
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157.
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158.
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Nonlinkage of 16q markers to familial predisposition to Wilms' tumor. [electronic resource] by
- Huff, V
- Reeve, A E
- Leppert, M
- Strong, L C
- Douglass, E C
- Geiser, C F
- Li, F P
- Meadows, A
- Callen, D F
- Lenoir, G
Producer: 19921118
In:
Cancer research vol. 52
Availability: No items available.
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159.
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High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome. [electronic resource] by
- Fang, Y Y
- Bain, S
- Haan, E A
- Eyre, H J
- MacDonald, M
- Wright, T J
- Altherr, M R
- Riess, O
- Sutherland, G
- Callen, D F
Producer: 19971007
In:
American journal of medical genetics vol. 71
Availability: No items available.
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160.
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Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9. [electronic resource] by
- Wang, Z Y
- Qiu, Q Q
- Seufert, W
- Taguchi, T
- Testa, J R
- Whitmore, S A
- Callen, D F
- Welsh, D
- Shenk, T
- Deuel, T F
Producer: 19961125
In:
The Journal of biological chemistry vol. 271
Availability: No items available.
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