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The Journal of Urology|November 21, 2002
Genitourinary malformations in chromosome 22q11.2 deletionHsi-Yang Wu, Susan L Rusnack, Richard D Bellah, et al.Molecular Cytogenetics|August 5, 2022
Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphismDong Li, Alanna Strong, Cuiping Hou, et al.Neuropediatrics|March 13, 2023
Subdural Hemorrhage as an Early Presentation in a Case of Sotos SyndromeTomoki T Nomakuchi, Cesar Augusto P Alves, Lauren A Beslow, et al.American Journal of Medical Genetics|April 23, 1999
Jagged1 mutations in patients ascertained with isolated congenital heart defectsI D Krantz, R Smith, R P Colliton, et al.Journal of Clinical and Experimental Neuropsychology|January 10, 2002
The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memoryC E Bearden, M F Woodin, P P Wang, et al.Neurology|October 1, 1995
Brainstem tumors in patients with neurofibromatosis type 1: a distinct clinical entityP T Molloy, L T Bilaniuk, S N Vaughan, et al.American Journal of Medical Genetics. Part A|June 17, 2008
Intracytoplasmic sperm injection (ICSI) with transmission of a ring(Y) chromosome and ovotesticular disorder of sex development in offspringNancy B Spinner, Sulagna C Saitta, Daniel P Delaney, et al.American Journal of Medical Genetics. Part A|July 3, 2007
Atypical teratoid/rhabdoid tumor in a patient with Beckwith-Wiedemann syndromeEric M Jackson, Tamim H Shaikh, Fan Zhang, et al.Journal of Pediatric Orthopedics|October 27, 2004
Congenital scoliosis and vertebral malformations: characterization of segmental defects for genetic analysisBülent Erol, Michael R Tracy, John P Dormans, et al.Journal of Medical Genetics|October 1, 1993
High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotypeD F Callen, H Eyre, S Lane, et al.Pageof 63