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2221.
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Novel mutations in the GH gene (GH1) uncover putative splicing regulatory elements. [electronic resource] by
- Babu, Deepak
- Mellone, Simona
- Fusco, Ileana
- Petri, Antonella
- Walker, Gillian E
- Bellone, Simonetta
- Prodam, Flavia
- Momigliano-Richiardi, Patricia
- Bona, Gianni
- Giordano, Mara
Producer: 20140616
In:
Endocrinology vol. 155
Availability: No items available.
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2222.
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2223.
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2224.
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2225.
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Large-scale analysis of the Alu Ya5 and Yb8 subfamilies and their contribution to human genomic diversity. [electronic resource] by
- Carroll, M L
- Roy-Engel, A M
- Nguyen, S V
- Salem, A H
- Vogel, E
- Vincent, B
- Myers, J
- Ahmad, Z
- Nguyen, L
- Sammarco, M
- Watkins, W S
- Henke, J
- Makalowski, W
- Jorde, L B
- Deininger, P L
- Batzer, M A
Producer: 20010823
In:
Journal of molecular biology vol. 311
Availability: No items available.
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2226.
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2227.
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2228.
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2229.
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2230.
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Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus. [electronic resource] by
- Losekoot, M
- Hoogendoorn, E
- Olmer, R
- Jansen, C C
- Oosterwijk, J C
- van den Ouweland, A M
- Halley, D J
- Warren, S T
- Willemsen, R
- Oostra, B A
- Bakker, E
Producer: 19980130
In:
Journal of medical genetics vol. 34
Availability: No items available.
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2231.
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2232.
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2233.
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2234.
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2235.
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2236.
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2237.
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2238.
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2239.
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2240.
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