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Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome. [electronic resource] by
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- Lin, Shuan-Pei
- Chern, Schu-Rern
- Wu, Peih-Shan
- Chen, Yen-Ni
- Chen, Shin-Wen
- Yang, Chien-Wen
- Town, Dai-Dyi
- Lee, Meng-Shan
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Producer: 20181107
In:
Taiwanese journal of obstetrics & gynecology vol. 56
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Radiological Features in Patients with Short Stature Homeobox-Containing (SHOX) Gene Deficiency and Turner Syndrome before and after 2 Years of GH Treatment. [electronic resource] by
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- Quigley, Charmian A
- Zimmermann, Alan G
- Garding, Gina
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Producer: 20160513
In:
Hormone research in paediatrics vol. 84
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60.
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Genotype-Phenotype Relationship in Patients and Relatives with SHOX Region Anomalies in the French Population. [electronic resource] by
- Auger, Julie
- Baptiste, Amandine
- Benabbad, Imane
- Thierry, Gaëlle
- Costa, Jean-Marc
- Amouyal, Mélanie
- Kottler, Marie-Laure
- Leheup, Bruno
- Touraine, Renaud
- Schmitt, Sébastien
- Lebrun, Marine
- Cormier Daire, Valérie
- Bonnefont, Jean-Paul
- de Roux, Nicolas
- Elie, Caroline
- Rosilio, Myriam
Producer: 20170417
In:
Hormone research in paediatrics vol. 86
Availability: No items available.
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