Bramswig, N. C. Et Al. 2015. Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin–Siris and Nicolaides–Baraitser syndromes. Human Genetics , vol.134, no.6 , 553-568.

Bramswig, N. C., Luedecke, H., Alanay, Y., Albrecht, B., Barthelmie, A., Boduroglu, K., ... Braunholz, D.(2015). Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin–Siris and Nicolaides–Baraitser syndromes. Human Genetics , vol.134, no.6, 553-568.

Bramswig, PELİN Et Al. "Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin–Siris and Nicolaides–Baraitser syndromes," Human Genetics , vol.134, no.6, 553-568, 2015

Bramswig, PELİN Ö. Et Al. "Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin–Siris and Nicolaides–Baraitser syndromes." Human Genetics , vol.134, no.6, pp.553-568, 2015

Bramswig, N. C. Et Al. (2015) . "Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin–Siris and Nicolaides–Baraitser syndromes." Human Genetics , vol.134, no.6, pp.553-568.

@article{article, author={PELİN ÖZLEM ŞİMŞEK KİPER Et Al. }, title={Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin–Siris and Nicolaides–Baraitser syndromes}, journal={Human Genetics}, year=2015, pages={553-568} }