Published in Arch Dis Child Fetal Neonatal Ed on November 01, 1998
The origin and impact of embryonic aneuploidy. Hum Genet (2013) 1.25
Non-invasive prenatal chromosomal aneuploidy testing--clinical experience: 100,000 clinical samples. PLoS One (2014) 1.19
Effect of folate intake on health outcomes in pregnancy: a systematic review and meta-analysis on birth weight, placental weight and length of gestation. Nutr J (2012) 1.06
Prenatal exposure to traffic-related air pollution and ultrasound measures of fetal growth in the INMA Sabadell cohort. Environ Health Perspect (2010) 1.05
Diagnosis and management of fetal growth restriction. J Pregnancy (2011) 0.99
Discordant circulating fetal DNA and subsequent cytogenetics reveal false negative, placental mosaic, and fetal mosaic cfDNA genotypes. J Transl Med (2015) 0.77
Could Digital PCR Be an Alternative as a Non-Invasive Prenatal Test for Trisomy 21: A Proof of Concept Study. PLoS One (2016) 0.76
Maternal origin of 47,XXY and confined placental mosaicism 47,XXY/48,XXY,+13 in an infant conceived through IVF. J Assist Reprod Genet (2013) 0.75
Is obstetric and neonatal outcome worse in fetuses who fail to reach their own growth potential? Br J Obstet Gynaecol (1992) 3.83
Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism. Prenat Diagn (1991) 1.77
Chromosomal mosaicism confined to the placenta in human conceptions. Science (1983) 1.67
Cytogenetic results from the U.S. Collaborative Study on CVS. Prenat Diagn (1992) 1.35
Uniparental disomy for chromosome 16 in humans. Am J Hum Genet (1993) 1.33
Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction. Am J Hum Genet (1997) 1.21
Comparative genomic hybridization in clinical cytogenetics. Am J Hum Genet (1995) 1.15
Confined placental mosaicism. J Med Genet (1996) 1.12
European collaborative research on mosaicism in CVS (EUCROMIC)--fetal and extrafetal cell lineages in 192 gestations with CVS mosaicism involving single autosomal trisomy. Am J Med Genet (1997) 1.11
Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7. J Med Genet (1995) 1.08
The long-term outcome of retarded fetal growth. Clin Obstet Gynecol (1997) 1.04
Mosaicism and accuracy of prenatal cytogenetic diagnoses after chorionic villus sampling and placental biopsies. Prenat Diagn (1991) 1.01
Workshop summary: fetal growth: its regulation and disorders. Pediatrics (1997) 0.94
Incidence and outcome of chromosomal mosaicism found at the time of chorionic villus sampling. Am J Obstet Gynecol (1997) 0.93
Small for gestational age fetus and neonatal outcome: reevaluation of the relationship. Am J Perinatol (1995) 0.92
Mosaicism in chorionic villus sampling: an association with poor perinatal outcome. Obstet Gynecol (1990) 0.92
Classification schemes of small-for-gestational age and type of intrauterine growth retardation and its implications to early neonatal mortality. Early Hum Dev (1990) 0.91
Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios. Prenat Diagn (1997) 0.86
Confined placental mosaicism and intrauterine growth retardation: a case-control analysis of placentas at delivery. Am J Obstet Gynecol (1995) 0.86
The relationship of ponderal index and other measurements to birthweight in preterm neonates. J Perinat Med (1997) 0.85
Intra-uterine growth retardation. Curr Opin Obstet Gynecol (1996) 0.85
Uniparental disomy (UPD). Genomic imprinting and a case for new genetics (prenatal and clinical implications: the "Likon" concept). Ann Genet (1997) 0.84
Prenatal diagnosis of trisomy 9: cytogenetic, fish, and DNA studies. Prenat Diagn (1997) 0.84
Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative survey. Prenat Diagn (1994) 0.83
Confined placental mosaicism in term placentae: analysis of 125 cases. Prenat Diagn (1995) 0.79
Elevated alpha-fetoprotein and human chorionic gonadotropin as a marker for placental trisomy 16 in the second trimester? Prenat Diagn (1995) 0.77
Evidence for multi-site closure of the neural tube in humans. Am J Med Genet (1993) 2.16
Chromosomal mosaicism confined to the placenta in human conceptions. Science (1983) 1.67
Chromosome abnormalities of eighty-one pediatric germ cell tumors: sex-, age-, site-, and histopathology-related differences--a Children's Cancer Group study. Genes Chromosomes Cancer (1999) 1.53
Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions. Am J Hum Genet (2000) 1.50
Chromosome analysis of human oocytes failing to fertilize in vitro. Fertil Steril (1989) 1.47
Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction. Am J Hum Genet (1997) 1.21
Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies. Am J Hum Genet (2002) 1.20
Long-term marrow culture reveals chromosomally normal hematopoietic progenitor cells in patients with Philadelphia chromosome-positive chronic myelogenous leukemia. N Engl J Med (1983) 1.17
Unregulated proliferation of primitive chronic myeloid leukemia progenitors in the presence of normal marrow adherent cells. Proc Natl Acad Sci U S A (1986) 1.16
Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism. Am J Hum Genet (1997) 1.12
Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7. J Med Genet (1995) 1.08
A new translocation, t(10;14)(q24;q11), in T cell neoplasia. Blood (1986) 1.08
Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion. Hum Genet (1991) 1.07
Klinefelter's syndrome and acute leukemia. Cancer Genet Cytogenet (1987) 1.07
Two different phenotypes of fetuses with chromosomal triploidy: correlation with parental origin of the extra haploid set. Am J Med Genet (1991) 1.03
A family with Huntington disease and reciprocal translocation 4;5. Am J Hum Genet (1986) 1.02
Cytogenetic analysis of 109 pediatric central nervous system tumors. Cancer Genet Cytogenet (1993) 0.99
Embryoscopic and cytogenetic analysis of 233 missed abortions: factors involved in the pathogenesis of developmental defects of early failed pregnancies. Hum Reprod (2003) 0.96
Distribution of mosaicism in human placentae. Hum Genet (1996) 0.96
Effects of triploidy on early human development. Prenat Diagn (2004) 0.96
A method for obtaining high quality chromosome preparations from single hemopoietic colonies on a routine basis. Cancer Genet Cytogenet (1981) 0.95
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations. Prenat Diagn (1997) 0.94
Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies. Am J Med Genet (2002) 0.93
Interphase cytogenetic analysis of single cell suspensions prepared from previously formalin-fixed and paraffin-embedded tissues. Mod Pathol (1995) 0.92
Anatomic and chromosome anomalies in specimens of early spontaneous abortion: seven-year experience. Birth Defects Orig Artic Ser (1987) 0.91
Cytogenetic studies of early myeloid progenitor compartments in Ph1-positive chronic myeloid leukaemia (CML). I. Persistence of Ph1-negative committed progenitors that are suppressed from differentiating in vivo. Br J Haematol (1984) 0.91
Successful autografting in chronic myeloid leukaemia after maintenance of marrow in culture. Bone Marrow Transplant (1989) 0.89
Cytogenetic findings in over 2000 amniocenteses. Can Med Assoc J (1983) 0.88
Neural tube defects: heterogeneity and homogeneity. Am J Med Genet Suppl (1986) 0.88
Altered smooth muscle development and innervation in the lower genitourinary and gastrointestinal tract of the male human fetus with myelomeningocele. J Urol (1998) 0.86
Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios. Prenat Diagn (1997) 0.86
Screening of human placentas for chromosomal mosaicism using comparative genomic hybridization. Teratology (1999) 0.86
Deletion of the short arms of chromosome 20. Hum Genet (1976) 0.86
Mild phenotypic abnormalities in combined del 9p2 and dup 3p2. Am J Med Genet (1990) 0.85
Transient myeloproliferative disorder in chromosomally normal newborn infant. Med Pediatr Oncol (1987) 0.85
Detection of confined placental mosaicism in trisomy 18 conceptions using interphase cytogenetic analysis. Hum Genet (1993) 0.85
Variable persistence of leukemic progenitor cells in long-term CML and AML marrow cultures. Kroc Found Ser (1984) 0.84
Molecular analysis of clonality and bcr rearrangements in Philadelphia chromosome-positive acute lymphoblastic leukemia. Blood (1988) 0.84
Nonclonal hemopoietic progenitors in a G6PD heterozygote with chronic myelogenous leukemia revealed after long-term marrow culture. Am J Hematol (1987) 0.84
X chromosome aneuploidy in lymphocyte cultures from women with recurrent spontaneous abortions. Am J Med Genet (1987) 0.84
The utilization of interphase cytogenetic analysis for the detection of mosaicism. Hum Genet (1994) 0.84
Cytogenetic and molecular genetic analysis of a pediatric pleomorphic sarcoma reveals similarities to adult malignant fibrous histiocytoma. Cancer Genet Cytogenet (1997) 0.83
Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicism. J Med Genet (2003) 0.83
Further delineation of X-linked mental retardation. Hum Genet (1981) 0.83
Comparative genomic hybridization: a new approach to screening for intrauterine complete or mosaic aneuploidy. Am J Med Genet (2000) 0.82
Childhood myelodysplasia: suggested classification as myelodysplastic syndromes based on laboratory and clinical findings. Am J Pediatr Hematol Oncol (1990) 0.82
Fluorodeoxyuridine synchronization of hemopoietic colonies. Cancer Genet Cytogenet (1987) 0.81
Interstitial 7q deletion [46,XX,del(7)(pter----q21.1::q22----qter)] and the location of genes for beta-glucuronidase and cystic fibrosis. Am J Med Genet (1988) 0.81
The early amniocentesis study: a randomized clinical trial of early amniocentesis versus midtrimester amniocentesis. Fetal Diagn Ther (1996) 0.81
Confined placental mosaicism for chromosome 7 detected by comparative genomic hybridization. Prenat Diagn (1998) 0.81
An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta. Clin Genet (2000) 0.81
Morphologic, immunologic, and cytogenetic classification of acute myeloid leukemia and myelodysplastic syndrome in childhood: a report from the Childrens Cancer Group. Leukemia (1996) 0.81
Nonclonal hemopoietic progenitor cells detected in long-term marrow cultures from a Turner syndrome mosaic with chronic myeloid leukemia. Blood (1984) 0.81
Lymphatic abnormalities in fetuses with posterior cervical cystic hygroma. Am J Med Genet (1989) 0.80
Acute myelomonocytic leukemia (AML-M4) and translocation t(6;9)(p23);q34): two additional patients with prominent myelodysplasia. Am J Hematol (1987) 0.80
Investigation of effects of pregnant mare serum gonadotropin (PMSG) on the chromosomal complement of CD-1 mouse embryos. J Assist Reprod Genet (1997) 0.80
Transcervical embryoscopy in missed abortion. J Assist Reprod Genet (2001) 0.79
Prenatally detected trisomy 20 mosaicism. Prenat Diagn (2005) 0.79
Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. chromosome mosaicism in CVS and amniocentesis samples. Prenat Diagn (1992) 0.79
Molecular cytogenetic detection of confined gonadal mosaicism in a conceptus with trisomy 16 placental mosaicism. Am J Hum Genet (1998) 0.79
Karyotypic analysis of two related cervical carcinoma cell lines that contain human papillomavirus type 18 DNA and express divergent differentiation. Cancer Genet Cytogenet (1989) 0.79
Chromosome investigation in in vitro fertilization failure. J Assist Reprod Genet (1994) 0.78
The chromosome pattern of embryos derived from tripronuclear zygotes studied by cytogenetic analysis and fluorescence in situ hybridization. Fertil Steril (1995) 0.78
Analysis of nine pregnancies with confined placental mosaicism for trisomy 2. Prenat Diagn (1996) 0.78
Pathology of abortion: chromosomal and genetic correlations. Monogr Pathol (1991) 0.77
Cytogenetic findings in 318 couples with repeated spontaneous abortion: a review of experience in British Columbia. Am J Med Genet (1984) 0.77
Duplication of 9P and hyperplasia of the choroid plexus: a pathologic, radiologic, and molecular cytogenetics study. Pediatr Pathol Lab Med (1997) 0.77
Mosaicism most likely accounts for extended survival of trisomy 22. Am J Med Genet (1996) 0.77
Partial molar pregnancy with fetal survival: an unusual example of confined placental mosaicism. Obstet Gynecol (1993) 0.76
Fetal akinesia deformation sequence in previable fetuses. Am J Med Genet (1988) 0.76
Bilateral renal agenesis with multiple congenital ocular anomalies. Am J Ophthalmol (1976) 0.76
Fragile X syndrome in autistic boys. J Autism Dev Disord (1989) 0.76
Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy. Prenat Diagn (2001) 0.76
Comparative genomic hybridization: a new tool for reproductive pathology. Arch Pathol Lab Med (2001) 0.75
Misconceptions about mosaicism. Prenat Diagn (1997) 0.75
Variable clinical expression of mosaic trisomy 16 in the newborn infant. Am J Med Genet (1994) 0.75
Further insights gained from diagnosis of two abnormal cell lines at amniocentesis. Prenat Diagn (1998) 0.75
Quality control in components of comparative genomic hybridization technique used for diagnostic cytogenetic analysis. Prenat Diagn (2000) 0.75
Amnion rupture sequence in a first trimester missed abortion. Prenat Diagn (2001) 0.75
The preliminary investigation (protocol) of the malformed fetus or neonate--or--what to do until the pathologist comes. Birth Defects Orig Artic Ser (1979) 0.75
Genetic causes of stillbirth. Semin Perinatol (1992) 0.75
Translocation t(3;5) in acute myelocytic leukemia type M2. Cancer Genet Cytogenet (1986) 0.75
Juvenile monosomy 7 syndrome: evidence that the disease originates in a pluripotent hemopoietic stem cell. Leuk Res (1987) 0.75
Transcervical fetoscopic diagnosis of structural defects in four first-trimester monochorionic twin intrauterine deaths. Prenat Diagn (2003) 0.75
Cytogenetic abnormalities among spontaneously aborted previable fetuses. Am J Med Genet Suppl (1987) 0.75
Detection and enumeration of colonic mucosal cells in amniotic fluid using a colon epithelial-specific monoclonal antibody. Prenat Diagn (1990) 0.75
Diagnostic pathologic investigation of the malformed conceptus. Perspect Pediatr Pathol (1982) 0.75
Congenital Wilms' tumor with metastasis. Pediatr Radiol (1976) 0.75
Metastatic infantile Wilms' tumor and hydrocephalus; a case report with review of the literature. Cancer (1977) 0.75
Chronic arthritis in two children with partial deletion of chromosome 18. J Rheumatol (1987) 0.75
Flow cytometric and karyotypic analyses of androgen-responsive and androgen-independent Shionogi mouse mammary tumours. Cell Biol Int Rep (1987) 0.75
Simultaneous appearance of a unique common epitope in fetal colon, skin, and biliary epithelial cells. A possible link for extracolonic manifestations in ulcerative colitis. J Clin Gastroenterol (1992) 0.75
Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. List of all cytogenetic abnormalities detected. Prenat Diagn (1992) 0.75
A co-twin fetus papyraceus as a cause of elevated AFP and acetylcholinesterase in the amniotic fluid of the normal co-twin. Pediatr Pathol (1991) 0.75
Translocation t(3;3)(q21;q26) and thrombocytosis. Cancer Genet Cytogenet (1986) 0.75
A routine method for cytogenetic analysis of small urinary bladder tumor biopsies. Cancer Genet Cytogenet (1987) 0.75
Neonate with Down's syndrome and transient congenital leukemia. In vitro studies. Am J Pediatr Hematol Oncol (1983) 0.75
Case 6. Adrenal hypoplasia in triploidy. Pediatr Pathol (1984) 0.75