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Rare copy number variants are a common cause of short stature. [electronic resource] by
- Zahnleiter, Diana
- Uebe, Steffen
- Ekici, Arif B
- Hoyer, Juliane
- Wiesener, Antje
- Wieczorek, Dagmar
- Kunstmann, Erdmute
- Reis, André
- Doerr, Helmuth-Guenther
- Rauch, Anita
- Thiel, Christian T
Producer: 20130613
In:
PLoS genetics vol. 9
Availability: No items available.
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Genotype-phenotype correlations in Noonan syndrome. [electronic resource] by
- Zenker, Martin
- Buheitel, Gernot
- Rauch, Ralf
- Koenig, Rainer
- Bosse, Kirstin
- Kress, Wolfram
- Tietze, Hans-Ulrich
- Doerr, Helmuth-Guenther
- Hofbeck, Michael
- Singer, Helmut
- Reis, André
- Rauch, Anita
Producer: 20040415
In:
The Journal of pediatrics vol. 144
Availability: No items available.
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SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome. [electronic resource] by
- Zenker, Martin
- Horn, Denise
- Wieczorek, Dagmar
- Allanson, Judith
- Pauli, Silke
- van der Burgt, Ineke
- Doerr, Helmuth-Guenther
- Gaspar, Harald
- Hofbeck, Michael
- Gillessen-Kaesbach, Gabriele
- Koch, Andreas
- Meinecke, Peter
- Mundlos, Stefan
- Nowka, Anja
- Rauch, Anita
- Reif, Silke
- von Schnakenburg, Christian
- Seidel, Heide
- Wehner, Lars-Erik
- Zweier, Christiane
- Bauhuber, Susanne
- Matejas, Verena
- Kratz, Christian P
- Thomas, Christoph
- Kutsche, Kerstin
Producer: 20071023
In:
Journal of medical genetics vol. 44
Availability: No items available.
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Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature. [electronic resource] by
- Hauer, Nadine N
- Popp, Bernt
- Taher, Leila
- Vogl, Carina
- Dhandapany, Perundurai S
- Büttner, Christian
- Uebe, Steffen
- Sticht, Heinrich
- Ferrazzi, Fulvia
- Ekici, Arif B
- De Luca, Alessandro
- Klinger, Patrizia
- Kraus, Cornelia
- Zweier, Christiane
- Wiesener, Antje
- Jamra, Rami Abou
- Kunstmann, Erdmute
- Rauch, Anita
- Wieczorek, Dagmar
- Jung, Anna-Marie
- Rohrer, Tilman R
- Zenker, Martin
- Doerr, Helmuth-Guenther
- Reis, André
- Thiel, Christian T
Producer: 20200611
In:
European journal of human genetics : EJHG vol. 27
Availability: No items available.
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