D. Manchester

T. Nelson, D. Pretorius, D. Manchester, 1988, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Dosimeters of human exposure to carcinogens: polycyclic aromatic hydrocarbon-macromolecular adducts.

B. Brooks, J. Willey, D. Mann, 1988, IARC scientific publications.

Determinants of polycyclic aromatic hydrocarbon-DNA adducts in human placenta.

E. Bowman, N. Caporaso, A. Weston, 1992, Cancer research.

Human Placental Microsomal Activation and DNA Adduction by Air Pollutants

A. Prahalad, D. Manchester, J. Gallagher, 1999, Bulletin of environmental contamination and toxicology.

Competitive binding of 7-substituted-2,3-dichlorodibenzo-p-dioxins with human placental ah receptor--a QSAR analysis.

T. Fujita, S. Safe, A. Okey, 1990, Biochemical pharmacology.

7-substituted-2,3-dichlorodibenzo-p-dioxins as competitive ligands for the Ah receptor : quantitative structure-activity relationships (QSARs) and a comparison of human receptor with Ah receptor from rodents

T. Fujita, S. Safe, A. Okey, 1990 .

Lymphedema in Noonan syndrome: Clues to pathogenesis and prenatal diagnosis and review of the literature

J. Opitz, H. Hoyme, J. Fryns, 1987, American journal of medical genetics.

Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three- and four-probe multicolor FISH in sperm.

A. Wyrobek, D. Manchester, X. Lowe, 1997, American journal of human genetics.

The clinical significance of increased echogenicity in the fetal abdomen.

D. Pretorius, M. Manco-Johnson, W. Clewell, 1985, AJR. American journal of roentgenology.

Ethnic variability in the allelic distribution of human aryl hydrocarbon receptor codon 554 and assessment of variant receptor function in vitro.

R. Tyndale, E. Sellers, U. Meyer, 2001, Pharmacogenetics.

Clinical course of fetal hydrocephalus: 40 cases.

D. Pretorius, M. Manco-Johnson, W. Clewell, 1985, AJR. American journal of roentgenology.

CYP 1 A 1 Messenger RNA Levels in Placental Tissue as a Biomarker of Environmental Exposure 1

F. Perera, W. Tsai, D. Bell, 2005 .

Possible association between maternal indomethacin therapy and primary pulmonary hypertension of the newborn.

H. Margolis, R. E. Sheldon, D. Manchester, 1976, American journal of obstetrics and gynecology.

Synchronous fluorescence spectroscopic, immunoaffinity chromatographic and 32P-postlabeling analysis of human placental DNA known to contain benzo[a]pyrene diol epoxide adducts.

C. Harris, D. Mann, V. Wilson, 1990, Carcinogenesis.

Derivative fluorescence spectral analysis of polycyclic aromatic hydrocarbon-DNA adducts in human placenta.

C. Harris, D. Mann, G. Trivers, 1989, Chemical research in toxicology.

Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development.

C. Richards, S. Patil, A. Taylor, 1999, American journal of medical genetics.

Importance of the Clinical Recognition of Loeys-Dietz Syndrome in the Neonatal Period

D. Ivy, D. Manchester, A. Yetman, 2007, Pediatrics.

Parental somatic and germ-line mosaicism for a multiexon deletion with unusual endpoints in a type III collagen (COL3A1) allele produces Ehlers-Danlos syndrome type IV in the heterozygous offspring.

P. Byers, D. Milewicz, Ann C M Smith, 1993, American journal of human genetics.

Perinatal Autopsy: Its Clinical Value

W. Clewell, D. Manchester, R. Shikes, 1986, Obstetrics and gynecology.

An outbreak of rotavirus-associated neonatal necrotizing enterocolitis*

R. Yolken, M. Levin, H. Rotbart, 1983, The Journal of Pediatrics.

Relationship between ambient air pollution and DNA damage in Polish mothers and newborns.

F P Perera, W Jedrychowski, S J Garte, 1998, Environmental health perspectives.

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.

C Eng, K. Lunetta, C. Romano, 1999, Human molecular genetics.

Fetal omphalocele and gastroschisis: a review of 24 cases.

D. Pretorius, M. Manco-Johnson, P. Russ, 1986, AJR. American journal of roentgenology.

Fluorescence and mass spectral evidence for the formation of benzo[a]pyrene anti-diol-epoxide-DNA and -hemoglobin adducts in humans.

P B Farmer, C. Harris, D. Mann, 1989, Carcinogenesis.

Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.

W. Dobyns, E. Andermann, R. Guerrini, 1998, Human molecular genetics.

Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

J. Rosenfeld, P. Stankiewicz, P. Szafranski, 2017, Human Genetics.

Specific skeletal dysplasias in utero: sonographic diagnosis.

D. Pretorius, M. Manco-Johnson, W. Clewell, 1986, Radiology.

Accuracy of ultrasound diagnoses in pregnancies complicated by suspected fetal anomalies

D. Pretorius, M. Manco-Johnson, W. Clewell, 1988, Prenatal diagnosis.

Biallelic Mutations in the 3’ Exonuclease TOE1 Cause Pontocerebellar Hypoplasia and Uncover a Role in snRNA Processing

Gene W. Yeo, S. Gabriel, F. Baas, 2016, Nature Genetics.

Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.

E. Zackai, A. Guttmacher, M. Bamshad, 2005, American journal of human genetics.

Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes

J. Rosenfeld, B. Torchia, L. Shaffer, 2011, European Journal of Human Genetics.

Harnessing genomics to identify environmental determinants of heritable disease.

M. Hurles, J. Lupski, P. Awadalla, 2013, Mutation research.

Tracheoesophageal fistula in utero. Twenty‐two cases.

D. Pretorius, M. A. Dennis, M. Manco-Johnson, 1987, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Severe polyhydramnios: incidence of anomalies.

T. Nelson, D. Pretorius, M. Manco-Johnson, 1987, AJR. American journal of roentgenology.

Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy

E. Bertini, M. Simpson, H. Goebel, 2012, Nature Genetics.

Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails

K. Winston, R. Keating, D. Manchester, 2012, Child's Nervous System.

Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q.

M. Cohen, L. Mcgavran, K. Prescott, 1994, American journal of medical genetics.

Molecular Epidemiology: Dosimetry, Susceptibility, and Cancer Risk

E. Bowman, C. Harris, P. Shields, 1990 .

Detection of Carcinogen–Macromolecular Adducts in Humans

C. C. Harris, A. Weston, D. Manchester, 1989 .

Recent developments in molecular epidemiology: A study of the effects of environmental polycyclic aromatic hydrocarbons on birth outcomes in Poland.

F. Perera, R. Ottman, R. Santella, 1998, American journal of epidemiology.

Polycyclic aromatic hydrocarbon-DNA adducts in human placenta and modulation by CYP1A1 induction and genotype.

F P Perera, W Jedrychowski, S J Garte, 1998, Carcinogenesis.

Ventriculomegaly: evaluation and management.

D. Pretorius, M. Manco-Johnson, W. Clewell, 1985, Seminars in perinatology.

Mutations in the δ-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)

E. Hoffman, D. Manchester, C. Hart, 1997, Neurogenetics.

Twin study methodology and variability in xenobiotic placental metabolism.

D. Manchester, K. Gottlieb, 1986, Teratogenesis, carcinogenesis, and mutagenesis.

Two massive congenital intracranial immature teratomas with neck extension.

B. Kleinschmidt-DeMasters, D. Manchester, S. Rostad, 1985, Teratology.

Detection of polycyclic aromatic hydrocarbon-DNA adducts in human lung.

E. Bowman, P. Shields, G. Trivers, 1993, Environmental health perspectives.

Monoclonal antibody phenotyping of interindividual differences in cytochrome P-450-dependent reactions of single and twin human placenta.

R. Tarone, D. Manchester, H. Gelboin, 1984, Cancer research.

Diagnosis and management of fetal hydrocephalus.

M. Manco-Johnson, W. Clewell, D. Manchester, 1986 .

The application of immunoassays and fluorometry to the detection of polycyclic hydrocarbon-macromolecular adducts and anti-adduct antibodies in humans

C. Harris, D. Mann, A. Haugen, 1988, International archives of occupational and environmental health.

Recurrent maternal floor infarction: a preventable cause of fetal death.

W. Clewell, D. Manchester, 1983, American journal of obstetrics and gynecology.

Sensitivity of somatic mutations in human umbilical cord blood to maternal environments

R. Albertini, J. Nicklas, J. O’Neill, 1995, Environmental and molecular mutagenesis.

Apparent Smith-Lemli-Opitz syndrome and Miller-Dieker syndrome in a family with segregating translocation t(7;17)(q34;p13.1).

R. Berry, R. Porreco, D. Manchester, 1989, American journal of medical genetics.

Diagnosis and Management of Fetal Hydrocephalus

M. Manco-Johnson, W. Clewell, D. Manchester, 1986, Clinical obstetrics and gynecology.

Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

J. Rosenfeld, P. Stankiewicz, P. Szafranski, 2017, Human Genetics.

Fetal Heart Rate in Relation to Body Mass

G. Meschia, F. Battaglia, D. Manchester, 1983, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Resolution and reconstitution of human placental monooxygenase activity responsive to maternal cigarette smoking.

D. Manchester, E. Jacoby, 1982, Developmental pharmacology and therapeutics.

Use of the Internet by patients and their families to obtain genetics-related information.

A. Alman, D. Manchester, Matthew R.G. Taylor, 2001, Mayo Clinic proceedings.