Results
|
|
2221.
|
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.
|
|
|
2222.
|
|
|
|
2223.
|
|
|
|
2224.
|
|
|
|
2225.
|
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.
|
|
|
2226.
|
|
|
|
2227.
|
|
|
|
2228.
|
|
|
|
2229.
|
|
|
|
2230.
|
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.
|
|
|
2231.
|
|
|
|
2232.
|
|
|
|
2233.
|
|
|
|
2234.
|
|
|
|
2235.
|
|
|
|
2236.
|
|
|
|
2237.
|
|
|
|
2238.
|
|
|
|
2239.
|
|
|
|
2240.
|
|