Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3)

Publisher： Karger

E-ISSN： 1424-859x|150|1|29-34

ISSN： 1424-8581

Source： Cytogenetic and Genome Research, Vol.150, Iss.1, 2016-11, pp. : 29-34

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Petits ARN C/D et syndrome de Prader-Willi

By Vitali Patrice Cavaillé Jérôme

Médecine/sciences, Vol. 21, Iss. 12, 2010-11 ,pp. : 1017-1019

Edp Sciences

Access to resources Recommend Favorite

Unbalanced 1q Whole-Arm Translocation Resulting in der(14)t(1;14)(q11–12;p11) in Myelodysplastic Syndrome

Cytogenetic and Genome Research, Vol. 136, Iss. 4, 2012-05 ,pp. : 256-263

Karger

Access to resources Recommend Favorite

Pure Trisomy 2p Syndrome in Two Siblings with an Unbalanced Translocation and Minimal Terminal 12q Monosomy Characterized by High-Density Microarray

Cytogenetic and Genome Research, Vol. 142, Iss. 4, 2014-04 ,pp. : 249-254

Karger

Access to resources Recommend Favorite

Identification and molecular characterization of de novo translocation t(8;14)(q22.3;q13) associated with a vascular and tissue overgrowth syndrome

Cytogenetic and Genome Research, Vol. 95, Iss. 3-4, 2002-06 ,pp. : 183-188

Karger

Access to resources Recommend Favorite

Le syndrome de Prader-Willi en 2015

By Tauber Maïthé Thuilleaux Denise Bieth Éric

Médecine/sciences, Vol. 31, Iss. 10, 2015-10 ,pp. : 853-860

Edp Sciences

Access to resources Recommend Favorite