The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients

Biological properties of prolactin-releasing peptide analogs with a modified aromatic ring of a C-terminal phenylalanine amide

(2011) Lenka Maletínská et al.   PEPTIDES

Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems

(2010) Stephen R. Williams et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism

(2010) Françoise Devillard et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Molecular characterization of a new patient with a non-recurrent inv dup del 2q and review of the mechanisms for this rearrangement

(2010) Ascensión Vera-Carbonell et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Partial 6p trisomy associated with infantile autism

(2010) Larry Burd et al.   CLINICAL GENETICS

Roles of prolactin-releasing peptide and RFamide related peptides in the control of stress and food intake

(2010) Yuki Takayanagi et al.   FEBS Journal

Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy ofMSX2with craniosynostosis

(2009) Ariana Kariminejad et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome

(2009) Bärbel Felder et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Two cases of deletion 2q37 associated with segregation of an unbalanced translocation 2;21: choanal atresia leading to misdiagnosis of CHARGE syndrome

(2009) Eduardo Fernández-Rebollo et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Bronchiectasis and immune deficiency in an adult patient with deletion 2q37 due to an unbalanced translocation t(2;10)

(2009) Irina Balikova et al.   European Journal of Medical Genetics

Array-CGH in patients with Kabuki-like phenotype: Identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration

(2008) Ivon Cuscó et al.   BMC Medical Genetics

Deletion 2q37: An Identifiable Clinical Syndrome With Mental Retardation and Autism

(2008) Cinzia Galasso et al.   JOURNAL OF CHILD NEUROLOGY