Neurodevelopmental profile of a new dysmorphic syndrome associated with submicroscopic partial deletion of 1p36.3

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes1999 · 72 citations
2. 2Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature1999 · 41 citations
3. 3Partial monosomy of chromosome 1p36.3: Characterization of the critical region and delineation of a syndrome1995 · 52 citations
4. 4Etiologic and Pathogenetic Study of Mental Retardation with Multiple Congenital Anomalies1992 · 7 citations
5. 5Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.1995 · 58 citations