Stress and coping in families of children with Smith-Magenis syndromeHODAPP, R. M; FIDLER, D. J; SMITH, A. C. M et al.JIDR. Journal of intellectual disability research (Print). 1998, Vol 42, Num 5, pp 331-340, issn 0964-2633Article

Behavioral phenotype of smith-magenis syndrome (del 17p11.2)SMITH, A. C. M; DYKENS, E; GREENBERG, F et al.American journal of medical genetics. 1998, Vol 81, Num 2, pp 179-185, issn 0148-7299Article

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeLO NIGRO, C; CHONG, S. S; SMITH, A. C. M et al.Human molecular genetics (Print). 1997, Vol 6, Num 2, pp 157-164, issn 0964-6906Article

Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3POLLIN, T. I; DOBYNS, W. B; CROWE, C. A et al.American journal of medical genetics. 1999, Vol 85, Num 4, pp 369-375, issn 0148-7299Conference Paper

Distinctiveness and correlates of maladaptive behaviour in children and adolescents with Smith-Magenis syndromeDYKENS, E. M; SMITH, A. C. M.JIDR. Journal of intellectual disability research (Print). 1998, Vol 42, Num 6, pp 481-489, issn 0964-2633Article

Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues : implication for prenatal diagnosisKUBOTA, T; ARADHYA, S; LEDBETTER, D. H et al.Journal of medical genetics. 1996, Vol 33, Num 12, pp 1011-1014, issn 0022-2593Article

Autism, mental retardation, and chromosomal abnormalitiesMARINER, R; JACKSON, A. W. III; LEVITAS, A et al.Journal of autism and developmental disorders. 1986, Vol 16, Num 4, pp 425-440, issn 0162-3257Article

Molecular analysis of the Smith-Magenis syndrome : a possible contiguous-gene syndrome associated with del(17)(p11.2)GREENBERG, F; GUZZETTA, V; MONTES DE OTA-LUNA, R et al.American journal of human genetics. 1991, Vol 49, Num 6, pp 1207-1218, issn 0002-9297Article

Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndromeTHIBODEAU, S. N; DORKINS, H. R; FAULK, K. R et al.Human genetics. 1988, Vol 79, Num 3, pp 219-227, issn 0340-6717Article

Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the hispanic population of the southwestern United StatesSMITH, A. C. M; SPUHLER, K; WILLIAMS, T. M et al.American journal of human genetics. 1987, Vol 41, Num 6, pp 1083-1103, issn 0002-9297Article

Clinicopathologic and dysmorphic findings in recombinant chromosome 8 syndromeWILLIAMS, T. M; MCCONNELL, T. S; MARTINEZ, F. JR et al.Human pathology. 1984, Vol 15, Num 11, pp 1080-1084, issn 0046-8177Article

Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 casesEDELMAN, E. A; GIRIRAJAN, S; FINUCANE, B et al.Clinical genetics. 2007, Vol 71, Num 6, pp 540-550, issn 0009-9163, 11 p.Article

Association of sex chromosome anomalies with childhood-onset psychotic disordersKUMRA, S; WIGGS, E; KRASNEWICH, D et al.Journal of the American Academy of Child and Adolescent Psychiatry. 1998, Vol 37, Num 3, pp 292-296, issn 0890-8567Article

Parental somatic and germ-line moisaicism for a multiexon deletion with unusual endpoints in a type III collagen (COL3AI) allele produces Ehlers-Danlos syndrome type IV in the heterozygous offspringMCGOOKEY MILEWICZ, D; WITZ, A. M; SMITH, A. C. M et al.American journal of human genetics. 1993, Vol 53, Num 1, pp 62-70, issn 0002-9297Article

Natural history of the recombinant (8) syndromeSUJANSKY, E; SMITH, A. C. M; PRESCOTT, K. E et al.American journal of medical genetics. 1993, Vol 47, Num 4, pp 512-525, issn 0148-7299Article

Monozygotic twin girls with congenital malformations resembling fanconi anemiaPOOLE, S. R; SMITH, A. C. M; HAYS, T et al.American journal of medical genetics. 1992, Vol 42, Num 6, pp 780-784, issn 0148-7299Article

The face of Smith-Magenis syndrome : a subjective and objective studyALLANSON, J. E; GREENBERG, F; SMITH, A. C. M et al.Journal of medical genetics. 1999, Vol 36, Num 5, pp 394-397, issn 0022-2593Article

Sleep disturbance in smith-magenis syndrome (del 17 p11.2)SMITH, A. C. M; DYKENS, E; GREENBERG, F et al.American journal of medical genetics. 1998, Vol 81, Num 2, pp 186-191, issn 0148-7299Article

A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3CHONG, S. S; PACK, S. D; ROSCHKE, A. V et al.Human molecular genetics (Print). 1997, Vol 6, Num 2, pp 147-155, issn 0964-6906Article

Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicismCHRISTIAN, S. L; SMITH, A. C. M; LEDBETTER, D. H et al.Prenatal diagnosis. 1996, Vol 16, Num 4, pp 323-332, issn 0197-3851Article

Institutional screening for the fragile X syndromeHAGERMAN, R; BERRA, R; JACKSON, A. W. III et al.American journal of diseases of children (1960). 1988, Vol 142, Num 11, pp 1216-1221, issn 0002-922XArticle

Interstitial deletion of (17)(p11.2p11.2) in nine patientsSMITH, A. C. M; MCGAVRAN, L; ROBINSON, J et al.American journal of medical genetics. 1986, Vol 24, Num 3, pp 393-414, issn 0148-7299Article