Synthesis of 3,5,12-triazawurtzitanes (3,5,12-triazatetracyclo[5.3.1.1^2,6.0^4,9]dodecanes)NIELSEN, A. T; CHRISTIAN, S. L; MOORE, D. W et al.Journal of organic chemistry. 1987, Vol 52, Num 9, pp 1656-1662, issn 0022-3263Article

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

Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndromeKUBOTA, T; SUTCLIFFE, J. S; ARADHYA, S et al.American journal of medical genetics. 1996, Vol 66, Num 1, pp 77-80, issn 0148-7299Article

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patientsCHRISTIAN, S. L; ROBINSON, W. P; HUANG, B et al.American journal of human genetics. 1995, Vol 57, Num 1, pp 40-48, issn 0002-9297Article

B-chronic lymphocytic leukemia cells contain both endogenous κ immunoglobulin mRNA and critical immunoglobulin gene activation transcription factorsZAKNOEN, S. L; CHRISTIAN, S. L; SUEN, R et al.Leukemia. 1992, Vol 6, Num 7, pp 675-679, issn 0887-6924Article

Singleton deletions throughout the genome increase risk of bipolar disorderZHANG, D; CHENG, L; SMITH, E. N et al.Molecular psychiatry. 2009, Vol 14, Num 4, pp 376-380, issn 1359-4184, 5 p.Article

Targets of B-cell antigen receptor signaling : the phosphatidylinositol 3-kinase/akt/glycogen synthase kinase-3 signaling pathway and the Rap 1 gtpaseGOLD, M. R; INGHAM, R. J; MCLEOD, S. J et al.Immunological reviews. 2000, Vol 176, pp 47-68, issn 0105-2896Article

Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasiaSPIRO, R. P; CHRISTIAN, S. L; LEDBETTER, D. H et al.Pediatric research. 1999, Vol 46, Num 5, pp 510-513, issn 0031-3998Article

Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndromeSUTCLIFFE, J. S; HAN, M; CHRISTIAN, S. L et al.Lancet (British edition). 1997, Vol 350, Num 9090, pp 1520-1521, issn 0140-6736Article

Synthesis of tetranitrotoluenesNIELSEN, A. T; CHRISTIAN, S. L; CHAFIN, A. P et al.Journal of organic chemistry. 1994, Vol 59, Num 7, pp 1714-1718, issn 0022-3263Article

In vitro and in vivo comparison of viral and cellular internal ribosome entry sites for bicistronic vector expressionLICURSI, M; CHRISTIAN, S. L; PONGNOPPARAT, T et al.Gene therapy (Basingstoke). 2011, Vol 18, Num 6, pp 631-636, issn 0969-7128, 6 p.Article

Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal mellitusCHRISTIAN, S. L; RICH, B. H; LOEBL, C et al.The Journal of pediatrics. 1999, Vol 134, Num 1, pp 42-46, issn 0022-3476Article

Molecular screening for proximal 15q abnormalities in a mentally retarded populationJACOBSEN, J; KING, B. H; LEVENTHAL, B. L et al.Journal of medical genetics. 1998, Vol 35, Num 7, pp 534-538, issn 0022-2593Article

Robertsonian (15q;15q) translocation in a child with Angelman syndrome : Evidence of uniparental disomyTONK, V; SCHULTZ, R. A; CHRISTIAN, S. L et al.American journal of medical genetics. 1996, Vol 66, Num 4, pp 426-428, issn 0148-7299Article

Nitrocarbons. IV: Reaction of polynitrobenzenes with hydrogen halides. Formation of polynitrohalobenzenesNIELSEN, A. T; CHAFIN, A. P; CHRISTIAN, S. L et al.Journal of organic chemistry. 1984, Vol 49, Num 24, pp 4575-4580, issn 0022-3263Article

Disruption of contactin 4 in three subjects with autism spectrum disorderROOHI, J; MONTAGNA, C; TEGAY, D. H et al.Journal of medical genetics. 2009, Vol 46, Num 3, pp 176-182, issn 0022-2593, 7 p.Article

Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15ROBINSON, W. P; CHRISTIAN, S. L; KUCHINKA, B. D et al.Clinical genetics. 2000, Vol 57, Num 5, pp 349-358, issn 0009-9163Article

The spectrum of mutations in UBE3A causing Angelman syndromePING FANG; LEV-LEHMAN, E; LANGLOIS, S et al.Human molecular genetics (Print). 1999, Vol 8, Num 1, pp 129-135, issn 0964-6906Article

Two 22q telomere deletions serendipitously detected by FISHPRECHT, K. S; LESE, C. M; SPIRO, R. P et al.Journal of medical genetics. 1998, Vol 35, Num 11, pp 939-942, issn 0022-2593Article

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

Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal originPAULYSON, K. J; SHERER, D. M; CHRISTIAN, S. L et al.Prenatal diagnosis. 1996, Vol 16, Num 11, pp 1021-1026, issn 0197-3851Article

Organisation of the pericentromeric region of chromosome 15: at east four partial gene copies are amplified in patients with a proximal duplication of 15qFANTES, J. A; MEWBORN, S. K; LESE, C. M et al.Journal of medical genetics. 2002, Vol 39, Num 3, pp 170-177, issn 0022-2593Article

Maternal meiosis I non-disjunction of chromosome 15 : dependence of the maternal age effect on level of recombinationROBINSON, W. P; KUCHINKA, B. D; SCHUFFENHAUER, S et al.Human molecular genetics (Print). 1998, Vol 7, Num 6, pp 1011-1019, issn 0964-6906Article

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomesHUANG, B; CROLLA, J. A; CHRISTIAN, S. L et al.Human genetics. 1997, Vol 99, Num 1, pp 11-17, issn 0340-6717Article

A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 11q11q13BUTLER, M. G; CHRISTIAN, S. L; KUBOTA, T et al.American journal of medical genetics. 1996, Vol 65, Num 2, pp 137-141, issn 0148-7299Article