Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader–Willi syndrome

Recognizing the unique prenatal phenotype of Prader‐Willi Syndrome ( PWS ) indicates the need for a diagnostic methylation test

(2020) Naama Srebnik et al.   PRENATAL DIAGNOSIS

Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound

(2018) Chih-Ping Chen et al.   Taiwanese Journal of Obstetrics & Gynecology

Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1 , NIPA2 , CYFIP1 , and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay

(2017) Chih-Ping Chen et al.   Taiwanese Journal of Obstetrics & Gynecology

Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot

(2016) Chih-Ping Chen et al.   Taiwanese Journal of Obstetrics & Gynecology

Meis2 is essential for cranial and cardiac neural crest development

(2015) Ondrej Machon et al.   BMC DEVELOPMENTAL BIOLOGY

De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s

(2012) Elena Rossi et al.   PLoS One

Further evidence for the possible role ofMEIS2in the development of cleft palate and cardiac septum

(2010) Moira A. Crowley et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

15q13q14 deletions: Phenotypic characterization and molecular delineation by comparative genomic hybridization

(2008) Nicola Brunetti-Pierri et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Prader-Willi syndrome: is there a recognizable fetal phenotype?

(2008) Nicole Bigi et al.   PRENATAL DIAGNOSIS