S. Elias

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Folic Acid for the Prevention of Neural Tube Defects

C. Moore, B. Pletcher, C. Cunniff, 1999, Pediatrics.

Amniocentesis and Fetal Blood Sampling

S. Elias, 2010 .

Parental decision following prenatal diagnosis of fetal chromosome abnormality.

J. Simpson, S. Elias, M. Verp, 1988, American journal of medical genetics.

Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data

K. Klinger, L. Sullivan, W. Holzgreve, 2002, Prenatal diagnosis.

Medical Fetal Therapy

S. Elias, O. Phillips, 1993 .

Isolation and genetic analysis of fetal nucleated red blood cells from maternal blood: the Baylor College of Medicine experience.

F. Bischoff, J. Simpson, S. Elias, 1996, Early human development.

Culture of fetal cells from maternal blood for prenatal diagnosis.

S. Elias, Hélène A. Elicha Gussin, 2002, Human reproduction update.

Studies of cystic fibrosis in Hutterite families by using linked DNA probes.

C. Ober, T. Laffler, S. Elias, 1987, American journal of human genetics.

Techniques for Prenatal Diagnosis

L. Shulman, S. Elias, 2013, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics.

Isolated fetal choroid plexus cysts and trisomy 18: a review and meta-analysis.

J. Simpson, L. Shulman, S. Elias, 1995, American journal of obstetrics and gynecology.

Amniocentesis Performed at 14 Weeks' Gestation or Earlier: Comparison With First‐Trimester Transabdominal Chorionic Villus Sampling

L. Shulman, S. Elias, O. Phillips, 1994, Obstetrics and gynecology.

Identification of a serum protein polymorphism via two-dimensional electrophoresis. Family and population studies in two genetically isolated groups: North American Hutterites and Australian aborigines.

C. Ober, S. Refetoff, S. Elias, 1991, American journal of human genetics.

Cancers of the breast and female genital system: search for recessive genetic factors through analysis of human isolate.

J. Simpson, G. Sarto, S. Elias, 1981, American journal of obstetrics and gynecology.

Prenatal diagnosis of genetic skin disease using fetal skin biopsy samples.

K. Holbrook, S. Elias, L. Smith, 1993, Archives of dermatology.

Interlaboratory comparison of fetal male DNA detection from common maternal plasma samples by real-time PCR.

K. Klinger, J. Vidaver, W. Holzgreve, 2004, Clinical chemistry.

Genetic analysis of HLA in the U.S. Schmiedenleut Hutterites.

C. Ober, S. Elias, D. Dawson, 1989, American journal of human genetics.

Lack of heritability in ovarian germ cell malignancies.

S. Wachtel, J. Simpson, L. Shulman, 1994, American journal of obstetrics and gynecology.

HLA associations in endometriosis.

J. Simpson, S. Carson, S. Elias, 1984, American journal of obstetrics and gynecology.

Second‐trimester maternal serum alpha‐fetoprotein screening of pregnancies characterized by first‐trimester isolated prominent fetal nuchal translucencies and normal karyotype

L. Shulman, S. Elias, S. Gross, 1995, Prenatal diagnosis.

Clinical course and outcome of fetuses with isolated cystic nuchal lesions and normal karyotypes detected in the first trimester.

L. Shulman, S. Elias, S. Gross, 1994, American journal of obstetrics and gynecology.

Prenatal Diagnosis with Fetal Cells Isolated From Maternal Blood by Multiparameter Flow Cytometry

K. Klinger, D. Shook, S. Wachtel, 1991, American journal of obstetrics and gynecology.

Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies.

J. Simpson, S. Carson, G. Sarto, 1983, Fertility and sterility.

Deficit of HLA homozygotes in a Caucasian isolate.

C. Ober, S. Elias, D. Dawson, 1993, Human immunology.

Transvaginal chorionic villus sampling using transabdominal ultrasound guidance: a new technique for first-trimester prenatal diagnosis.

J. Simpson, L. Shulman, S. Elias, 1993, Fetal diagnosis and therapy.

Endothelial Precursor Cells in the Peripheral Blood of Pregnant Women

R. Hoffman, F. Bischoff, S. Elias, 2002, The Journal of the Society for Gynecologic Investigation: JSGI.

Unexplained elevated maternal serum alpha-fetoprotein is not predictive of adverse perinatal outcome in an indigent urban population.

B. Sibai, J. Simpson, L. Shulman, 1992, American journal of obstetrics and gynecology.

Analysis of HLA haplotype segregation in the Schmiedeleut Hutterites of South Dakota.

C. Ober, S. Elias, D. Dawson, 1994, Human heredity.

Separation of Noncutaneous Epithelia in a Fetus Diagnosed In Utero with Junctional Epidermolysis Bullosa

K. Holbrook, Lynne T. Smith, S. Elias, 1992, Pediatric Research.

Second-Trimester Pregnancy Termination by Dilation and Evacuation After Detection of Fetal Abnormalities

L. Shulman, S. Elias, 1992 .

Fetal cells in maternal blood: NIFTY clinical trial interim analysis

L. Sullivan, W. Holzgreve, L. Jackson, 1999 .

Prenatal diagnosis by use of fetal cells isolated from maternal blood.

K. Klinger, S. Kaplan, W. Holzgreve, 1995, American journal of obstetrics and gynecology.

Fetal Cells in Maternal Blood: Prospects for Noninvasive Prenatal Diagnosis. Proceedings of a conference. Arlington, Virginia, September 27-29, 1993.

J. Simpson, S. Elias, 1994, Annals of the New York Academy of Sciences.

Low maternal serum α-fetoprotein and perinatal outcome

G. Somes, J. Simpson, S. Elias, 1987 .

Maternal serum α-fetoprotein screening: Low and high values for detection of genetic abnormalities☆☆☆

C. Ober, J. Simpson, S. Elias, 1986 .

Fetus-placenta-newborn☆

J. Haddow, G. Palomaki, B. Sibai, 1995 .

Associations between adverse perinatal outcome and serially obtained second- and third-trimester maternal serum alpha-fetoprotein measurements.

J. Haddow, G. Palomaki, B. Sibai, 1995, American journal of obstetrics and gynecology.

Second trimester maternal serum human chorionic gonadotropin and unconjugated oestriol levels in blacks and whites

L. Shulman, S. Elias, R. Andersen, 1990, The Lancet.

Analysis for amniotic fluid crystallization in second-trimester amniocentesis.

J. Simpson, S. Elias, A. Martin, 1979, American journal of obstetrics and gynecology.

Heritable aspects of uterine anomalies. II. Genetic analysis of Müllerian aplasia.

J. Simpson, S. Carson, G. Sarto, 1983, Fertility and sterility.

Short communications normal fetal growth despite persistent amniotic fluid leakage after genetic amniocentesis

S. Elias, M. Socol, S. Aladjem, 1981, Prenatal diagnosis.

Culture of endothelial cells isolated from maternal blood using anti‐CD105 and CD133

S. Elias, Arun K. Sharma, Hélène A. Elicha Gussin, 2004, Prenatal diagnosis.

Cytogenetic analysis of a case of "13q- syndrome" (46,XX,del 13) using banding techniques.

J. Simpson, S. Elias, L. Wilson, 1980, Journal of pediatric ophthalmology and strabismus.

Alpha‐fetoprotein and acetylcholinesterase are not predictive of fetal junctional epidermolysis bullosa, Herlitz variant

K. Holbrook, L. Shulman, S. Elias, 1991, Prenatal diagnosis.

Applicability of 19–DEJ‐l monoclonal antibody for the prenatal diagnosis or exclusion of junctional epidermolysis bullosa

K. Holbrook, S. Elias, J. Fine, 1990, Prenatal diagnosis.

Prenatal diagnosis of harlequin ichthyosis

M. Mazur, R. Sabbagha, S. Elias, 1980, Clinical genetics.

Use of fetoscopy for the prenatal diagnosis of hereditary skin disorders.

S. Elias, 1987, Current problems in dermatology.

Maternal serum screening for fetal genetic disorders.

S. Elias, H. L. Ross, 1997, Obstetrics and gynecology clinics of North America.

Adverse perinatal outcome in patients screen‐positive for neural tube defects and fetal down syndrome

L. Shulman, S. Elias, S. Gross, 1994, Prenatal diagnosis.

Decreased fecundability in Hutterite couples sharing HLA-DR.

W. Hauck, C. Ober, C. Ober, 1992, American journal of human genetics.

Human leukocyte antigen matching and fetal loss: results of a 10 year prospective study.

W. Hauck, C. Ober, C. Ober, 1998, Human reproduction.

Fetal Cells in Maternal Blood

S. Elias, J. Simpson, 1994 .

Prenatal effects of maternal-fetal HLA compatibility.

C. Ober, J. Simpson, R. Sabbagha, 1987, American journal of reproductive immunology and microbiology : AJRIM.

Fetomaternal transfusion depends on amount of chorionic villi aspirated but not on method of chorionic villus sampling.

J. Simpson, L. Shulman, S. Elias, 1990, American journal of obstetrics and gynecology.

Isolating fetal cells from maternal blood. Advances in prenatal diagnosis through molecular technology.

J. Simpson, S. Elias, J. Simpson, 1993, JAMA.

HLA sharing and fertility in Hutterite couples: evidence for prenatal selection against compatible fetuses.

W. Hauck, C. Ober, S. Elias, 1988, American journal of reproductive immunology and microbiology : AJRIM.

Prenatal diagnosis of congenital muscular dystrophy producing arthrogryposis.

J. Simpson, R. Tamura, R. Sabbagha, 1985, The New England journal of medicine.

Antenatal diagnosis of genodermatoses.

S. Elias, N. Esterly, Nancy B. Esterly, 1983, Journal of the American Academy of Dermatology.

Fetal cranial and craniocervical masses: ultrasound characteristics and differential diagnosis.

R. Tamura, R. Sabbagha, S. Elias, 1980, American journal of obstetrics and gynecology.

Amniocentesis and chorionic villus sampling.

L. Shulman, S. Elias, 1993, The Western journal of medicine.

Detection of chromosomal aneuploidy in endometriosis by multi-color fluorescence in situ hybridization (FISH)

F. Bischoff, J. Simpson, J. Shin, 1997, Human Genetics.

of a sporadic, unstable

S. Elias, S. Edward, Alice Martin, 2022 .

Does unexplained second-trimester (15 to 20 weeks' gestation) maternal serum alpha-fetoprotein elevation presage adverse perinatal outcome? Pitfalls and preliminary studies with late second- and third-trimester maternal serum alpha-fetoprotein.

B. Sibai, L. Shulman, B. Mercer, 1991, American journal of obstetrics and gynecology.

Positive Serum Screening for Fetal Down Syndrome Does Not Predict Adverse Pregnancy Outcome in Absence of Fetal Aneuploidy

L. Shulman, S. Elias, N. Meyer, 1994, The Journal of the Society for Gynecologic Investigation: JSGI.

Does unexplained second‐trimester (15 to 20 weeks' gestation) maternal serum α‐fetoprotein elevation presage adverse perinatal outcome? Pitfalls and preliminary studies with late second‐ and third‐trimester maternal serum α‐fetoprotein

B. Sibai, J. Simpson, L. Shulman, 1992 .

Maternal Serum Screening for Fetal Down Syndrome in Women Less Than 35 Years of Age Using Alpha-Fetoprotein, hCG, and Unconjugated Estriol: A Prospective 2-Year Study

J. Simpson, L. Shulman, S. Elias, 1992, Obstetrics and gynecology.

Localization of the nucleolar organizer by computer-aided analysis of a variant no. 21 in a human isolate

Alice O. Martin, J. Simpson, M. Rzeszotarski, 1979, Human Genetics.

Adverse effects of human leukocyte antigen-DR sharing on fertility: a cohort study in a human isolate.

W. Hauck, C. Ober, J. Simpson, 1985, Fertility and sterility.

First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood

K. Klinger, S. Wachtel, J. Simpson, 1992, The Lancet.

Rare event selection of fetal nucleated erythrocytes in maternal blood by flow cytometry.

F. Bischoff, W. Schober, J. Simpson, 1996, Cytometry.

Value of Amniocentesis versus Fetal Tissue for Cytogenetic Analysis in Cases of Fetal Demise

L. Shulman, S. Elias, Jessica T. Greenberg, 2009, Fetal Diagnosis and Therapy.

Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization.

J. Simpson, L. Shulman, P. L. Gordon, 1995, American journal of medical genetics.

Translocations are infrequent among couples having repeated spontaneous abortions but no other abnormal pregnancies.

C. Ober, J. Simpson, S. Elias, 1989, Fertility and sterility.

Syndromes of camptodactyly, multiple ankylosis, facial anomalies, and pulmonary hypoplasia.

J. Simpson, S. Elias, L. Boelen, 1978, Birth defects original article series.

Significance of septations in isolated fetal cystic hygroma detected in the first trimester

L. Shulman, S. Elias, D. Emerson, 1994, Prenatal diagnosis.

PRENATAL DIAGNOSIS OF HEREDITARY SKIN DISORDERS

S. Elias, N. Esterly, 1981, Clinical obstetrics and gynecology.

Use of fluorescence in situ hybridization to detect trisomy 18 in the direct preparation of a chorionic villus biopsy

V. Park, S. Elias, Avirachan T. Tharapel, 1992, Prenatal diagnosis.

Heritable aspects of endometriosis. I. Genetic studies.

J. Simpson, S. Elias, V. Buttram, 1980, American journal of obstetrics and gynecology.

Developmental abnormalities of the female reproductive tract: Pathogenesis and nosology†

L. Shulman, S. Elias, 1988 .

Dilation and Evacuation for Second-Trimester Genetic Pregnancy Termination

L. Shulman, S. Elias, F. Ling, 1990, Obstetrics and gynecology.

First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency).

P. White, N. Laforgia, P. Speiser, 1990, The Journal of clinical endocrinology and metabolism.

Anaphase lag as the most likely mechanism for monosomy X in direct cytotrophoblasts but not in mesenchymal core cells from the same villi.

M. Qumsiyeh, J. Simpson, L. Shulman, 1990, Journal of medical genetics.

FALSE-NEGATIVE FINDING ON CHORIONIC VILLUS SAMPLING

Alice O. Martin, J. Simpson, D. Fortune, 1986, The Lancet.

Resorbed co‐twin as an explanation for discrepant chorionic villus results: Non‐mosaic 47,XX, +16 in villi (direct and culture) with normal (46,XX) amniotic fluid and neonatal blood

L. Shulman, S. Elias, A. Tharapel, 1989, Prenatal diagnosis.

Hypermodal cells, hypomodal cells, and repetitive abortions.

J. Simpson, S. Elias, A. Martin, 1986, Fertility and sterility.

Amniocentesis for prenatal diagnosis in twin gestation

S. Elias, A. Gerbie, Joe Leigh Sirnpson, 1980, Clinical genetics.

Isolating fetal cells in maternal circulation for prenatal diagnosis

S. Elias, J L Simpson, S Elias, 1994, Prenatal diagnosis.

Amniocentesis for antenatal diagnosis of genetic defects.

S. Elias, A. Gerbie, 1980, Clinics in obstetrics and gynaecology.

Evaluation of a Culture System for Enrichment of CD34+ Hematopoietic Progenitor Cells Present in Maternal Blood

F. Bischoff, J. Simpson, S. Elias, 2002, Fetal Diagnosis and Therapy.

Association of N-Acetyltransferase 2 (NAT2) genetic polymorphism resulting in decreased capacity to detoxify aromatic amines in women with endometriosis

F. Bischoff, J. Simpson, S. Elias, 1998 .

Diabetes in pregnancy, Northwestern University series (1977-1981). I. Prospective study of anomalies in offspring of mothers with diabetes mellitus.

J. Simpson, S. Elias, E. Ogata, 1983, American journal of obstetrics and gynecology.

Chorionic villus sampling: First trimester prenatal diagnosis

J. Simpson, S. Elias, A. Bombard, 1986, Indian journal of pediatrics.

The role of fetoscopy in antenatal diagnosis.

S. Elias, 1980, Clinics in obstetrics and gynaecology.

High Frequency of Cytogenetic Abnormalities in Fetuses With Cystic Hygroma Diagnosed in the First Trimester

L. Shulman, S. Elias, O. Phillips, 1992, Obstetrics and gynecology.

Segregation analysis and genetic counseling when both parents carry balanced chromosomal translocations.

J. Simpson, L. Shulman, S. Elias, 1991, Fertility and sterility.

Prenatal Genetic Counseling Issues in Women of Advanced Reproductive Age

S. Elias, O. Phillips, 1993 .

Prenatal diagnosis with use of fetal cells isolated from maternal blood: five-color fluorescent in situ hybridization analysis on flow-sorted cells for chromosomes X, Y, 13, 18, and 21.

F. Bischoff, W. Schober, J. Simpson, 1998, American journal of obstetrics and gynecology.

Isolating fetal nucleated red blood cells from maternal blood: The baylor experience—1995

F. Bischoff, S. Elias, D. Lewis, 1995, Prenatal diagnosis.

Increased heterogeneity of chromosome 17 aneuploidy in endometriosis.

F. Bischoff, J. Simpson, S. Elias, 1999, American journal of obstetrics and gynecology.

Prenatal counselling and diagnosis in progressively deforming osteogenesis imperfecta: A case of autosomal dominant transmission

L. Shulman, S. Elias, O. Phillips, 1991, Prenatal diagnosis.

HLA and mate choice in humans.

L R Weitkamp, N. Cox, C. Ober, 1997, American journal of human genetics.

Culture of Cells from Maternal Circulation, in Conditions Favoring Fetal Endothelial Cell Expansion, Does Not Facilitate the Preferential Expansion of Circulating Fetal Cells

S. Elias, H. Gussin, Arun K. Sharma, 2004, Fetal Diagnosis and Therapy.

Ultrasonic induction of sister chromatid exchanges in human lymphocytes

Alice O. Martin, J. Simpson, R. Sabbagha, 1981, Human Genetics.

Endometrial adenocarcinoma: genetic analysis suggesting heritable site-specific uterine cancer.

J. Simpson, L. Shulman, L. Smiley, 1992, Gynecologic oncology.

Transabdominal chorionic villus sampling for prenatal diagnosis

L. Shulman, S. Elias, S. Rowe, 1988 .

Transvaginal chorionic villus sampling using transabdominal ultrasound guidance

J. Simpson, L. Shulman, S. Elias, 1992, Prenatal diagnosis.

The association between chorionic villus sampling and preeclampsia

L. Shulman, W. Grobman, S. Elias, 2009, Prenatal diagnosis.

Early twin amniocentesis prior to 14 weeks' gestation

L. Shulman, S. Elias, O. Phillips, 1992, Prenatal Diagnosis.

High‐resolution two‐dimensional electrophoretic survey of serum protein genetic types in Schmiedeleut Hutterites

C. Ober, S. Elias, K. Miller, 1991, American journal of human biology : the official journal of the Human Biology Council.

Chorionic villus sampling.

L. Shulman, S. Elias, 1989, Pediatric annals.

Chorionic villus sampling in continuing pregnancies. I. Low fetal loss rates in initial 109 cases.

J. Simpson, R. Sabbagha, S. Elias, 1986, American journal of obstetrics and gynecology.

Chorionic villus sampling for first-trimester prenatal diagnosis: Northwestern University program.

L. Keith, J. Simpson, R. Sabbagha, 1985, American journal of obstetrics and gynecology.

Genetic amniocentesis in twin gestations.

J. Simpson, R. Sabbagha, S. Elias, 1980, American journal of obstetrics and gynecology.

Detection of low‐grade mosaicism in fetal cells isolated from maternal blood

F. Bischoff, S. Elias, J. Simpson, 1995, Prenatal diagnosis.

Intact fetal cells in maternal plasma: are they really there?

W. Holzgreve, F. Bischoff, L. Jackson, 2003, The Lancet.

Effect of Hispanic ethnicity on interpretation of maternal serum screening.

D. Waller, S. Elias, J. Byrne, 1997, Fetal diagnosis and therapy.

Severity of abnormality influences decision to terminate pregnancies affected with fetal neural tube defects.

J. Simpson, L. Shulman, S. Elias, 1994, Fetal diagnosis and therapy.

Chromosome analysis of ectopic human conceptuses.

J. Simpson, S. Elias, M. Lebeau, 1981, American journal of obstetrics and gynecology.

Genetics Studies in Incomplete Müllerian Fusion

J. Simpson, S. Carson, S. Elias, 1984, Obstetrics and gynecology.

Dilatation and evacuation is a preferable method of mid‐trimester genetic termination of pregency

L. Shulman, S. Elias, F. Ling, 1989, Prenatal diagnosis.

Sister chromatid exchange frequency in directly prepared cytotrophoblasts: demonstration of in vivo deoxyribonucleic acid damage in pregnant women who smoke cigarettes.

J. Simpson, L. Shulman, S. Elias, 1991, American journal of obstetrics and gynecology.

Autoantibodies and pregnancy history in a healthy population.

C. Ober, T. Karrison, S. Elias, 1993, American journal of obstetrics and gynecology.

Noninvasive Determination of Fetal RhD Status Using Fetal DNA in Maternal Serum and PCR

F. Bischoff, J. Simpson, K. Moise, 1999, The Journal of the Society for Gynecologic Investigation: JSGI.

Original ArticlesReview Article : Molecular Analysis to Assign Parental Origin and Distinguish De Novo i(2I q) From t(2I q2I q) in Two Down Syndrome Fetuses

L. Shulman, S. Elias, A. Tharapel, 1994, The Journal of the Society for Gynecologic Investigation: JSGI.

Maternal serum screening for fetal down syndrome using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated estriol in adolescents

J. Simpson, L. Shulman, S. Elias, 1993 .

Heritable aspects of endometriosis

J. Simpson, S. Elias, V. Buttram, 1980 .

Low maternal serum alpha-fetoprotein and perinatal outcome.

G. Somes, J. Simpson, S. Elias, 1987, American journal of obstetrics and gynecology.

Rapid chromosome analysis with the use of spontaneously dividing cells derived from umbilical cord blood (fetal and neonatal).

J. Simpson, S. Elias, H. H. Chang, 1989, American journal of obstetrics and gynecology.

Chorionic villus sampling in continuing pregnancies. II. Cytogenetic reliability.

J. Simpson, S. Elias, A. Martin, 1986, American journal of obstetrics and gynecology.

Heritage aspects of endometriosis. II. Clinical characteristics of familial endometriosis.

J. Simpson, S. Elias, V. Buttram, 1980, American journal of obstetrics and gynecology.

Marker chromosomes in gonadal dysgenesis : avoiding unnecessary surgery

S. Wachtel, J. Simpson, L. Shulman, 1992 .

Parental chromosomal rearrangements associated with repetitive spontaneous abortions.

J. Simpson, S. Elias, A. Martin, 1981, Fertility and sterility.

Failure to document fetal cells in maternal circulation using the Selypes-Lorencz “air-culture” cytogenetic technique

L. Shulman, S. Elias, J. Simpson, 1990, Human Genetics.

Preimplantation genetic diagnosis by comparative genomic hybridization.

S. Elias, 2001, The New England journal of medicine.

Fetal Cells in the Maternal Circulation: Isolation by Multiparameter Flow Cytometry and Confirmation by Polymerase Chain Reaction

S. Wachtel, J. Simpson, L. Shulman, 1991, Human reproduction.

Prenatal Diagnosis of Aneuploidy Using Fetal Cells Isolated from Maternal Blood University of Tennessee, Memphis Experience a

S. Elias, J. Simpson, 1994, Annals of the New York Academy of Sciences.

A Model System Using Fetal Hemoglobin to Distinguish Fetal Cells Enriched from Maternal Blood

V. Park, S. Elias, R. Bravo, 1994, Annals of the New York Academy of Sciences.

Stability of sex chromosome mosaicism.

J. Simpson, S. Elias, A. Martin, 1980, American journal of obstetrics and gynecology.

Single-Cell Genetic Diagnosis: Molecular Methods and Pitfalls

J. Simpson, S. Carson, J. Buster, 1994 .

Diagnosis of Trisomy 18 Using Spontaneously Dividing Cells from Fetal Umbilical Cord Blood: A Novel Approach for Rapid Late Second and Third Trimester Prenatal Diagnosis

L. Shulman, S. Elias, A. Tharapel, 1990, American journal of perinatology.

Direct analysis of uncultured cytotrophoblastic cells from second- and third-trimester placentas: An accurate and rapid method for detection of fetal chromosome abnormalities

J. Simpson, L. Shulman, S. Elias, 1990 .

Mode of Ascertainment is Critical in Assessing Safety of Percutaneous Umbilical Blood Sampling

L. Shulman, B. Mercer, B. Sibai, 1993, American journal of perinatology.

Hypermodal cells in amniotic fluid cultures: frequency, interpretation, and clinical significance.

S. Elias, M. Verp, J. Simpson, 1982, American journal of obstetrics and gynecology.

Prenatal treatment: medical and gene therapy in the fetus.

S. Elias, J. Johnson, 1988, Clinical obstetrics and gynecology.

Clinical Implications of Chromosomal Inversions

J. Simpson, S. Elias, R. Deddish, 2008 .

Clinical implications of chromosomal inversions. A pericentric inversion in No. 18 segregating in a family ascertained through an abnormal proband.

J. Simpson, S. Elias, A. Martin, 1983, American journal of perinatology.

The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities.

D. Ledbetter, J. Hobbins, H. Lubs, 1989, The New England journal of medicine.

Minimal fetomaternal transfusion in ultrasound‐guided fetal skin sampling

L. Shulman, S. Elias, O. Phillips, 1991, Prenatal diagnosis.

Percutaneous umbilical blood sampling, fetal skin sampling, and fetal liver biopsy.

L. Shulman, S. Elias, 1990, Seminars in perinatology.

Prenatal diagnosis of hematologic disorders.

S. Elias, O. Phillips, 1995, Clinical obstetrics and gynecology.

Genetic counseling and genetic services in obstetrics and gynecology: implications for educational goals and clinical practice.

J. Simpson, S. Elias, A. Martin, 1981, American journal of obstetrics and gynecology.

Ultrasound-Guided Fetal Skin Sampling for Prenatal Diagnosis of Genodermatoses

K. Holbrook, L. Shulman, S. Elias, 1994, Obstetrics and gynecology.

Low False-Positive Rate of Aneuploidy Detection Using Fetal Cells Isolated from Maternal Blood

K. Klinger, W. Holzgreve, L. Jackson, 1998, Fetal Diagnosis and Therapy.