• 4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
• A case of mosaic ring chromosome 4 with subtelomeric 4p deletion
• A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4
• A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p)
• An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature
• Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype
• Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature
• Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophy
• Familial cryptic translocation with del 4q34-->qter and dup 12pter-->p13 in sibs with tracheal stenosis: clinical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in
• Familial distal monosomy 3p26.3-pter with trisomy 4q32.2-qter, presenting with progressive ataxia, intellectual disability, and dysmorphic features
• Hypoplastic left heart in a female infant with partial trisomy 4q due to de novo 4;21 translocation
• Interstitial deletion 4q32-34 with ulnar deficiency: 4q33 may be the critical region in 4q terminal deletion syndrome
• Interstitial deletion of the distal long arm of chromosome 4
• Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation
• Isolated myocardial non-compaction in an infant with distal 4q trisomy and distal 1q monosomy
• Molecular characterization of a consistent 4.5-megabase deletion at 4q28 in prostate cancer cells
• Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
• Mosaicism for terminal deletion of 4q
• Partial monosomy 2p and partial trisomy 4q due to paternal translocation t(2;4)(p25.1;q31.3)
• Partial monosomy of long arm of chromosome 4 due to interstitial deletion
• PARTIAL TRISOMY 4p AND PARTIAL MONOSOMY 13q: CASE REPORT AND A LITERATURE REVIEW
• Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies
• Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15)
• Recombinant chromosome 4 with partial 4p deletion and 4q duplication inherited from paternal pericentric inversion
• Solid-phase minisequencing confirmed by FISH analysis in determination of gene copy number
• Subtelomeric Copy Number Variations: The Importance of 4p/4q Deletions in Patients with Congenital Anomalies and Developmental Disability
• Syndrome of terminal deletion of the long arm of chromosome 4. Apropos of a personal case with a review of the literature
• Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome
• The 4q-syndrome: delineation of the minimal critical region to within band 4q31
• The tale of a nail sign in chromosome 4q34 deletion syndrome
• Unbalanced t(4;11)(q32;q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromes
• Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings