The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant. (Q37058516)
Jump to navigation
Jump to search
scientific article published on 26 August 2015
Language | Label | Description | Also known as |
---|---|---|---|
English | The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant. |
scientific article published on 26 August 2015 |
Statements
The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant (English)
Helen V Firth
Han G Brunner
Evan E Eichler
Sarina G Kant
Jayne Y Hehir-Kwa
Marjolein H Willemsen
Bradley P Coe
Bert B A de Vries
Rolph Pfundt
Erica H Gerkes
David A Koolen
Gea Beunders
Pinella Failla
Katrin Linda
Nathalie Van der Aa
Hermine E Veenstra-Knol
Jessie H Conta
Sarah Dugan
Sara Halbach
Omar A Abdul-Rahman
Heather M Winesett
Wendy K Chung
Marguerite Dalton
Petia S Dimova
Katrina Prescott
Hui Z Zhang
Howard M Saal
Marjolijn C Jongmans
Alice S Brooks
Diane Masser-Frye
Jennifer R Friedman
Modupe A Sokunbi
Abhijit Dixit
DDD Study
Mary K Kukolich
Jesús Flórez
Elizabeth M Thompson
Gabriele Gillessen-Kaesbach
26 August 2015
1 reference
1 reference