Results
|
|
61.
|
|
|
|
62.
|
|
|
|
63.
|
|
|
|
64.
|
|
|
|
65.
|
|
|
|
66.
|
|
|
|
67.
|
|
|
|
68.
|
Y-chromosome microdeletions are not associated with SHOX haploinsufficiency. [electronic resource] by
- Chianese, C
- Lo Giacco, D
- Tüttelmann, F
- Ferlin, A
- Ntostis, P
- Vinci, S
- Balercia, G
- Ars, E
- Ruiz-Castañé, E
- Giglio, S
- Forti, G
- Kliesch, S
- Krausz, C
Producer: 20140616
In:
Human reproduction (Oxford, England) vol. 28
Availability: No items available.
|
|
|
69.
|
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity. [electronic resource] by
- Grigelioniene, G
- Schoumans, J
- Neumeyer, L
- Ivarsson, A
- Eklöf, O
- Enkvist, O
- Tordai, P
- Fosdal, I
- Myhre, A G
- Westphal, O
- Nilsson, N O
- Elfving, M
- Ellis, I
- Anderlid, B M
- Fransson, I
- Tapia-Paez, I
- Nordenskjöld, M
- Hagenäs, L
- Dumanski, J P
Producer: 20011220
In:
Human genetics vol. 109
Availability: No items available.
|
|
|
70.
|
Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature. [electronic resource] by
- Rappold, Gudrun A
- Fukami, Maki
- Niesler, Beate
- Schiller, Simone
- Zumkeller, Walter
- Bettendorf, Markus
- Heinrich, Udo
- Vlachopapadoupoulou, Elpis
- Reinehr, Thomas
- Onigata, Kazumichi
- Ogata, Tsutomu
Producer: 20020408
In:
The Journal of clinical endocrinology and metabolism vol. 87
Availability: No items available.
|
|
|
71.
|
|
|
|
72.
|
Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhood. [electronic resource] by
- Flanagan, S F
- Munns, C F J
- Hayes, M
- Williams, B
- Berry, M
- Vickers, D
- Rao, E
- Rappold, G A
- Batch, J A
- Hyland, V J
- Glass, I A
Producer: 20021213
In:
Journal of medical genetics vol. 39
Availability: No items available.
|
|
|
73.
|
|
|
|
74.
|
|
|
|
75.
|
[The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study]. [electronic resource] by
- Dávid, Anna
- Butz, Henriett
- Halász, Zita
- Török, Dóra
- Nyirő, Gábor
- Muzsnai, Ágota
- Csákváry, Violetta
- Luczay, Andrea
- Sallai, Ágnes
- Hosszú, Éva
- Felszeghy, Enikő
- Tar, Attila
- Szántó, Zsuzsanna
- Fekete, Gy László
- Kun, Imre
- Patócs, Attila
- Bertalan, Rita
Producer: 20170928
In:
Orvosi hetilap vol. 158
Availability: No items available.
|
|
|
76.
|
SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome. [electronic resource] by
- Cormier-Daire, V
- Belin, V
- Cusin, V
- Viot, G
- Girlich, D
- Toutain, A
- Moncla, A
- Vekemans, M
- Le Merrer, M
- Munnich, A
Producer: 20000127
In:
Acta paediatrica (Oslo, Norway : 1992). Supplement vol. 88
Availability: No items available.
|
|
|
77.
|
|
|
|
78.
|
|
|
|
79.
|
|
|
|
80.
|
|