Publication

Amir RE, Van den Veyver IB, Schultz R, Malicki DM, Tran CQ, Dahle EJ, Philippi A, Timar L, Percy AK, Motil KJ, Lichtarge O, Smith EO, Glaze DG, Zoghbi HY, Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. Ann Neurol47:670-9 2000
PubMed ID: 10805343

Records Return:  (9) Show
 
Catalog IDGenderFamilyRelationshipDescription
GM11304Female1888probandRETT SYNDROME; RTT
GM11305Female1888motherRETT SYNDROME; RTT
GM11306Male1888fatherRETT SYNDROME; RTT
GM11301Female1887probandRETT SYNDROME; RTT
GM11302Female1887motherRETT SYNDROME; RTT
GM11303Male1887fatherRETT SYNDROME; RTT
GM11310Female1359probandRETT SYNDROME; RTT
GM11311Female1359motherRETT SYNDROME; RTT
GM11312Male1359fatherRETT SYNDROME; RTT