Preimplantation genetic testing for Huntington disease and certain other dominantly inherited disordersSCHULMAN, J. D; BLACK, S. H; HANDYSIDE, A et al.Clinical genetics. 1996, Vol 49, Num 2, pp 57-58, issn 0009-9163Article

Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicismKALOUSEK, D. K; HOWARD-PEEBLES, P. N; OLSON, S. B et al.Prenatal diagnosis. 1991, Vol 11, Num 10, pp 743-750, issn 0197-3851Article

The number of embryos available for transfer predicts successful pregnancy outcome in women over 39 years with normal ovarian hormonal reserve testingOPSAHL, M. S; BLAUER, K. L; BLACK, S. H et al.Journal of assisted reproduction and genetics. 2001, Vol 18, Num 10, pp 551-556, issn 1058-0468Article

Prenatal screening for ΔF₅₀₈ mutation in population not selected for cystic fibrosisBICK, D; MADDALENA, QA; BLACK, S. H et al.Lancet (British edition). 1990, Vol 336, Num 8726, pp 1324-1325, issn 0140-6736, 2 p.Article

Sjögren-Larsson syndrome: inherited defect in the fatty alcohol cycleRIZZO, W. B; DAMMANN, A. L; CRAFT, D. A et al.The Journal of pediatrics. 1989, Vol 115, Num 2, pp 228-234, issn 0022-3476Article

Pool boiling performance of finned surfaces in R-113ABUAF, N; BLACK, S. H; STAUB, F. W et al.International journal of heat and fluid flow. 1985, Vol 6, Num 1, pp 23-30, issn 0142-727XArticle

Uncooled Detector Development at RaytheonBLACK, S. H; SESSLER, T; GORDON, E et al.Proceedings of SPIE, the International Society for Optical Engineering. 2011, Vol 8012, issn 0277-786X, isbn 978-0-8194-8586-1, 80121A.1-80121A.12, 2Conference Paper

Births of normal daughters after MicroSort sperm separation and intrauterine insemination, in-vitro fertilization, or intracytoplasmic sperm injectionFUGGER, E. F; BLACK, S. H; KEYVANFAR, K et al.Human reproduction (Oxford. Print). 1998, Vol 13, Num 9, pp 2367-2370, issn 0268-1161Article

Mental retardation and ullrich-turner syndrome in cases with 45,X/46,X,+mar : additional support for the loss of the X-inactivation center hypothesisCOLE, H; BING HUANG; SALBERT, B. A et al.American journal of medical genetics. 1994, Vol 52, Num 2, pp 136-145, issn 0148-7299Article

Improved sizing of fragile X CGG repeats by nested polymerase chain reactionLEVINSON, G; MADDALENA, A; PALMER, F. T et al.American journal of medical genetics. 1994, Vol 51, Num 4, pp 527-534, issn 0148-7299Article

Rare non-mosaic trisomies in chorionic villus tissue not confirmed at amniocentesisDORFMANN, A. D; PERSZYK, J; ROBINSON, P et al.Prenatal diagnosis. 1992, Vol 12, Num 11, pp 899-902, issn 0197-3851Article

Preimplantation genetic diagnosis in Marfan syndromeKILPATRICK, M. W; HARTON, G. L; PHYLACTOU, L. A et al.Fetal diagnosis and therapy. 1996, Vol 11, Num 6, pp 402-406, issn 1015-3837Article

Molecular fragile X screening in normal populationsSPENCE, W. C; BLACK, S. H; FALLON, L et al.American journal of medical genetics. 1996, Vol 64, Num 1, pp 181-183, issn 0148-7299Article

Prenatal diagnosis of Sjögren-Larsson syndrome using enzymatic methodsRIZO, W. B; CRAFT, D. A; KELSON, T. L et al.Prenatal diagnosis. 1994, Vol 14, Num 7, pp 577-581, issn 0197-3851Article

Transvaginal chorionic villus samplingSIDRANSKY, E; BLACK, S. H; SOENKSEN, D. M et al.Prenatal diagnosis. 1990, Vol 10, Num 9, pp 583-586, issn 0197-3851, 4 p.Article

Prenatal sampling and bicornuate uterusBLACK, S. H; SCHULMAN, J. D.Prenatal diagnosis. 1988, Vol 8, Num 6, pp 476-477, issn 0197-3851Article

Efficiency of MicroSort flow cytometry for producing sperm populations enriched in X- or Y-chromosome haplotypes : a blind trial assessed by double and triple colour fluorescent in-situ hybridizationVIDAL, F; FUGGER, E. F; SCHULMAN, J. D et al.Human reproduction (Oxford. Print). 1998, Vol 13, Num 2, pp 308-312, issn 0268-1161Article

DNA-based X-enriched sperm separation as an adjunct to preimplantation genetic testing for the prevention of X-linked diseaseLEVINSON, G; KEYVANFAR, K; CALVO, L et al.Human reproduction (Oxford. Print). 1995, Vol 10, Num 4, pp 979-982, issn 0268-1161Article

Nucleated erythrocytes in maternal blood : quantity and quality of fetal cell in enriched populationsREADING, J. P; HUFFMAN, J. L; MENAPACE-DREW, G. F et al.Human reproduction (Oxford. Print). 1995, Vol 10, Num 9, pp 2510-2515, issn 0268-1161Article

Comparison of hepatitis B virus subtyping of d/y determinants by radioimmunoprecipitation assay and the polymerase chain reactionNICHOLSON, W. J; BLACK, S. H; SIMMONDS, P et al.Journal of medical virology. 1992, Vol 36, Num 1, pp 21-27, issn 0146-6615Article

Maroteaux-Lamy syndrome in a large consanguineous kindred: biochemical and immunological studiesBLACK, S. H; PELIAS, M. Z; MILLER, J. B et al.American journal of medical genetics. 1986, Vol 25, Num 2, pp 273-279, issn 0148-7299Article

Advances in High Rate Uncooled Detector Fabrication at RaytheonBLACK, S. H; KRAFT, R; MEDRANO, A et al.Proceedings of SPIE, the International Society for Optical Engineering. 2010, Vol 7660, issn 0277-786X, isbn 978-0-8194-8124-5, 76600X.1-76600X.12, 2Conference Paper

Disinfection by-product formation in swimming pool waters : A simple mass balanceJUDD, S. J; BLACK, S. H.Water research (Oxford). 2000, Vol 34, Num 5, pp 1611-1619, issn 0043-1354Article

Preimplantation genetic diagnosis for spinal muscular atrophy type IFALLON, L; HARTON, G. L; BICK, D et al.Neurology. 1999, Vol 53, Num 5, pp 1087-1090, issn 0028-3878Article

Fragile X premutation is a significant risk factor for premature ovarian failure : The international collaborative POF in fragile X study : Preliminary dataALLINGHAM-HAWKINS, D. J; BABUL-HIRJI, R; JENKINS, E. C et al.American journal of medical genetics. 1999, Vol 83, Num 4, pp 322-325, issn 0148-7299Article