Mitotic recombination among acrocentric chromosomes' short armsGIUSSANI, U; FACCHINETTI, B; CASSINA, G et al.Annals of human genetics. 1996, Vol 60, pp 91-97, issn 0003-4800, 2Article

Skeletal anomalies and deformities in patients with deletions of 22q11MING, J. E; MCDONALD-MCGINN, D. M; MEGERIAN, T. E et al.American journal of medical genetics. 1997, Vol 72, Num 2, pp 210-215, issn 0148-7299Article

Deletion of 22q11.2KATES, Wendy R; EMANUEL, Beverly S.Developmental disabilities research reviews. 2008, Vol 14, Num 1, 76 p.Serial Issue

Increased incidence of renal anomalies in patients with chromosome 22q11 microdeletionSTEWART, T. L; IRONS, M. B; COWAN, J. M et al.Teratology (Philadelphia, PA). 1999, Vol 59, Num 1, pp 20-22, issn 0040-3709Article

Juvenile rheumatoid arthritis and del(22q11) syndrome : a non-random associationVERLOES, A; CURRY, C; JAMAR, M et al.Journal of medical genetics. 1998, Vol 35, Num 11, pp 943-947, issn 0022-2593Article

Kabuki (Niikawa-Kuroki) syndrome associated with immunodeficiencyCHRZANOWSKA, K. H; KRAJEWSKA-WALASEK, M; KUS, J et al.Clinical genetics. 1998, Vol 53, Num 4, pp 308-312, issn 0009-9163Article

Another critical region for deletion of 22q11 : A study of 100 patientsKURAHASHI, H; TSUDA, E; KOHAMA, R et al.American journal of medical genetics. 1997, Vol 72, Num 2, pp 180-185, issn 0148-7299Article

Deletion of chromosome 22q11 and pseudohypoparathyroidismCRAIGEN, W. J; LINDSAY, E. A; BRICKER, J. T et al.American journal of medical genetics. 1997, Vol 72, Num 1, pp 63-65, issn 0148-7299Article

Thymoma with a t(15;22)(q11;q11)DAL CIN, P; DE WOLF-PEETERS, C; DENEFFE, G et al.Cancer genetics and cytogenetics. 1996, Vol 89, Num 2, pp 181-183, issn 0165-4608Article

GENETIC COUNSELING FOR THE 22Q11.2 DELETIONMCDONALD-MCGINN, Donna M; ZACKAI, Elaine H.Developmental disabilities research reviews. 2008, Vol 14, Num 1, pp 69-74, 6 p.Article

Molecular pathogenesis of Philadelphia chromosome negative myeloproliferative disordersKRALOVICS, Robert; SKODA, Radek C.Blood reviews. 2005, Vol 19, Num 1, pp 1-13, issn 0268-960X, 13 p.Article

Allelic variations at the haploid TBX1 locus do not influence the cardiac phenotype in cases of 22q11 microdeletionVOELCKEL, Marie-Antoinette; GIRARDOT, Lydie; GIUSIANO, Bernard et al.Annales de génétique (Paris). 2004, Vol 47, Num 3, pp 235-240, issn 0003-3995, 6 p.Article

Deletion 22q11 : A newly recognized cause of Behavioral and psychiatric disordersMCCANDLESS, S. E; SCOTT, J. A; ROBIN, N. H et al.Archives of pediatrics & adolescent medicine. 1998, Vol 152, Num 5, pp 481-484, issn 1072-4710Article

Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiencyZORI, R. T; BOYAR, F. Z; DIXON-WOOD, V et al.American journal of medical genetics. 1998, Vol 77, Num 1, pp 8-11, issn 0148-7299Article

Cat eye syndrome chromosome breakpoint clustering : identification of two intervals also associated with 22q11 deletion syndrome breakpointsMCTAGGART, K. E; BUDARF, M. L; DRISCOLL, D. A et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 3-4, pp 222-228, issn 0301-0171Conference Paper

Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patientsDOHENY, K. F; MCDERMID, H. E; HARUM, K et al.Journal of medical genetics. 1997, Vol 34, Num 8, pp 640-644, issn 0022-2593Article

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions : a European collaborative studyRYAN, A. K; GOODSHIP, J. A; AURIAS, A et al.Journal of medical genetics. 1997, Vol 34, Num 10, pp 798-804, issn 0022-2593Article

Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndromeFRYBURG, J. S; LIN, K. Y; GOLDEN, W. L et al.American journal of medical genetics. 1996, Vol 62, Num 3, pp 274-275, issn 0148-7299Conference Paper

MOLECULAR MECHANISMS AND DIAGNOSIS OF CHROMOSOME 22Q11.2 REARRANGEMENTSEMANUEL, Beverly S.Developmental disabilities research reviews. 2008, Vol 14, Num 1, pp 11-18, 8 p.Article

Five new subjects with ring chromosome 22ISHMAEL, H. A; CATALDI, D; BEGLEITER, M. L et al.Clinical genetics. 2003, Vol 63, Num 5, pp 410-414, issn 0009-9163, 5 p.Article

Increased need for medical interventions in infants with velocardiofacial (deletion 22q11) syndromeHOPKIN, R. J; SCHORRY, E. K; BOFINGER, M et al.The Journal of pediatrics. 2000, Vol 137, Num 2, pp 247-249, issn 0022-3476Article

Evolution of latent hypoparathyroidism in familial 22q11 deletion syndromeCUNEO, B. F; DRISCOLL, D. A; GIDDING, S. S et al.American journal of medical genetics. 1997, Vol 69, Num 1, pp 50-55, issn 0148-7299Article

Another case of t(17;22)(q22;q13) in an infantile dermatofibrosarcoma protuberansPEDEUTOUR, F; LACOUR, J. P; PERRIN, C et al.Cancer genetics and cytogenetics. 1996, Vol 89, Num 2, pp 175-176, issn 0165-4608Article

La microdélétion du chromosome 22q11 chez l'enfant : à propos d'une série de 49 patients = Chromosome 22q11 microdeletion : a series of 49 childrenLEVY-MOZZICONACCI, A; LACOMBE, D; LEHEUP, B et al.Archives de pédiatrie (Paris). 1996, Vol 3, Num 8, pp 761-768, issn 0929-693XConference Paper

Networks of attention in children with the 22q11 deletion syndromeSOBIN, Christina; KILEY-BRABECK, Karen; DANIELS, Sarah et al.Developmental neuropsychology. 2004, Vol 26, Num 2, pp 611-626, issn 8756-5641, 16 p.Article