Contiguous ∼16 Mb 1p36 deletion: Dominant features of classical distal 1p36 monosomy with haplo-lethality

Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions

(2010) Jill A. Rosenfeld et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia

(2009) Carla S. D'Angelo et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Molecular characterization of a monosomy 1p36 presenting as an Aicardi syndrome phenocopy

(2009) Anne-Claire Bursztejn et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements

(2009) Carla S. D’Angelo et al.   HUMAN GENETICS

Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome

(2009) Svetlana A. Yatsenko et al.   HUMAN MOLECULAR GENETICS

Buffering of Segmental and Chromosomal Aneuploidies in Drosophila melanogaster

(2009) Per Stenberg et al.   PLoS Genetics

Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36

(2008) Shoji Saito et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Prenatal diagnosis of monosomy 1p36: A focus on brain abnormalities and a review of the literature

(2008) Philippe M. Campeau et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A new case of proximal monosomy 1p36, extending the phenotype

(2008) Sabine Rudnik-Schöneborn et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1–p23.1, 4q21.21–q22.1, 6q26–q27, and 21q2

(2008) William B. Dobyns et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Proximal interstitial 1p36 deletion syndrome: The most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2)

(2008) Keiko Shimojima et al.   BRAIN & DEVELOPMENT

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

(2008) Heather C. Mefford et al.   NEW ENGLAND JOURNAL OF MEDICINE

Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation

(2008) A. Battaglia et al.   PEDIATRICS