Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype [3]

American Journal of Human Genetics

Volumn 62, Issue 2, 1998, Pages 495-498

  Gottlieb, S ^a   Driscoll, D A ^a   Punnett, H H ^a   Sellinger, B ^a   Emanuel, B S ^a   Budarf, M L ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 10P; CHROMOSOME DELETION; CLINICAL ARTICLE; DIGEORGE SYNDROME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HETEROZYGOSITY; HUMAN; LETTER; MALE; PHENOTYPE; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME;

EID: 0031912717     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301718     Document Type: Letter

References (9)

1. IM Chumakov P Rigault IL Gall C Bellanne-Chantelot A Billault S Guillou P Soularue A YAC contig of the human genome Nature 377 1995 175 297
2. SCM Daw C Taylor M Kraman K Call J Mao S Schuffenhauer T Meitinger A common region of 10p deleted in DiGeorge and velocardiofacial syndromes Nat Genet 13 1996 458 460
3. DA Driscoll BS Emanuel DiGeorge and velocardiofacial syndromes: the 22q11 deletion syndrome Ment Retard Dev Dis Res Rev 2 1996 130 138
4. F Greenberg FFB Elder P Haffner H Northrup D Ledbetter Cytogenetic findings in a prospective series of patients with DiGeorge anomaly Am J Hum Genet 43 1988 605 611
5. F Greenberg C Valdes HM Rosenblatt JL Kirkland DH Ledbetter Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome J Pediatr 109 1986 489 492
6. T Hudson L Stein S Gerety J Ma A Castle J Silva D Slonim An STS-based map of the human genome Science 270 1995 1945 1954
7. A Lipson K Fagan A Colley P Colley G Sholler D Issacs RK Oates Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13—implications for cytogenetics and molecular biology Am J Med Genet 65 1996 304 308
8. G Monaco C Pignata E Rossi O Mascellaro S Cocozza F Ciccimarra DiGeorge anomaly associated with 10p deletion Am J Med Genet 39 1991 215 216
9. C Pignata A D'Agostino P Finelli M Fiore I Scotese E Cosentini C Cuomo Progressive deficiencies in blood T cells associated with a 10p12-13 interstitial deletion Clin Immunol Immunopathol 80 1996 9 15