Published in Am J Med Genet on January 01, 1989
Genetic factors in congenital diaphragmatic hernia. Am J Hum Genet (2007) 1.58
Absence makes the search grow longer. Am J Hum Genet (1996) 1.38
Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss. Eur J Hum Genet (2008) 1.10
Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27. Eur J Hum Genet (2014) 0.91
Identification of TCTE3 as a gene responsible for congenital diaphragmatic hernia using a high-resolution single-nucleotide polymorphism array. Pediatr Surg Int (2011) 0.76
Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locus. EMBO J (1988) 3.82
Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene. Am J Hum Genet (1996) 2.41
A chart of failure risk for noninvasive ventilation in patients with COPD exacerbation. Eur Respir J (2005) 2.39
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28. Am J Hum Genet (1997) 1.99
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients. Am J Hum Genet (1995) 1.78
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole. Am J Hum Genet (2000) 1.69
Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion. Am J Med Genet (1996) 1.67
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas. Prog Clin Biol Res (1989) 1.66
Antenatal ultrasound for fetal anomalies: importance of perinatal autopsy. Pediatr Pathol (1989) 1.50
Three cases of tetrasomy 9p. Am J Med Genet (2002) 1.47
The syndromes of hydatidiform mole. I. Cytogenetic and morphologic correlations. Am J Obstet Gynecol (1978) 1.47
Retracted Identification of mosaicism in Prader-Willi syndrome using fluorescent in situ hybridization. Am J Med Genet (1996) 1.45
The syndromes of hydatidiform mole. II. Morphologic evolution of the complete and partial mole. Am J Obstet Gynecol (1978) 1.35
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers. Am J Hum Genet (1990) 1.25
The physical organization of the human immunoglobulin heavy chain gene complex. EMBO J (1990) 1.21
Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype. Nat Genet (1994) 1.11
Polyhydramnios: ultrasonically detected prevalence and neonatal outcome. Obstet Gynecol (1987) 1.09
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations. Am J Hum Genet (1994) 1.08
Application of chromosomal microarray in the evaluation of abnormal prenatal findings. Clin Genet (2012) 1.08
Use of amniocentesis in preterm gestation with ruptured membranes. Obstet Gynecol (1984) 1.03
Complete moles have paternal chromosomes but maternal mitochondrial DNA. Hum Genet (1982) 1.01
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Prenat Diagn (1996) 1.01
Two discrete regions of deletion at 7q in uterine leiomyomas. Genes Chromosomes Cancer (1997) 0.99
Morphologic anomalies in triploid liveborn fetuses. Hum Pathol (1983) 0.98
Maternal haemoglobin concentration, haematocrit and renal handling of urate in pregnancies ending in the births of small-for-dates infants. Br J Obstet Gynaecol (1978) 0.98
The clinicopathologic profile of the partial hydatidiform mole. Obstet Gynecol (1982) 0.96
Inhibition of the glucose-6-phosphate transporter in oilseed rape (Brassica napus L.) plastids by acyl-CoA thioesters reduces fatty acid synthesis. Biochem J (2000) 0.94
Diurnal variation of serum urate in pregnancy. Br Med J (1977) 0.94
Uterine leiomyomas: cytogenetic and histologic profile. Obstet Gynecol (1992) 0.93
Apparently balanced t(1;7)(q21.3;q34) in an infant with Coffin-Siris syndrome. Am J Med Genet (1997) 0.93
Qualitative amniotic fluid volume determination by ultrasound: antepartum detection of intrauterine growth retardation. Am J Obstet Gynecol (1981) 0.93
Subtypes of odorant-binding proteins--heterologous expression and ligand binding. Eur J Biochem (1998) 0.93
Tetraploid partial hydatidiform moles: two cases with a triple paternal contribution and a 92,XXXY karyotype. Hum Genet (1986) 0.93
Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyomas. Genes Chromosomes Cancer (1995) 0.93
Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies. Hum Genet (2000) 0.92
Rapid assessment of fetal hemoglobin concentration with the HemoCue system. Obstet Gynecol (1990) 0.91
Nonrandom cytogenetic changes in leiomyomas of the female genitourinary tract. A report of 35 cases. Cancer Genet Cytogenet (1991) 0.89
Recurrent triploid and dispermic conceptions in patients with NLRP7 mutations. Placenta (2011) 0.87
The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndrome. Prenat Diagn (1997) 0.87
Cytogenetic and histologic correlation of peripheral nerve sheath tumors of soft tissue. Cancer Genet Cytogenet (1996) 0.86
The association between polyhydramnios and preterm delivery. Obstet Gynecol (1995) 0.86
Deletion 7q22 in uterine leiomyoma. A cytogenetic review. Cancer Genet Cytogenet (1993) 0.86
Hydatidiform mole: cytogenetically unusual cases and their implications for the present classification. Am J Obstet Gynecol (1987) 0.86
Genetics and biology of human ovarian teratomas. III. Cytogenetics and origins of malignant ovarian germ cell tumors. Cancer Genet Cytogenet (1992) 0.86
Noninvasive positive-pressure ventilation in ALS: predictors of tolerance and survival. Neurology (2006) 0.85
Complete (classic) hydatidiform mole with 46,XY karyotype of paternal origin. Hum Genet (1979) 0.85
Cryptic duplication of 12q24.33 --> qter in a child with Angelman syndrome-simultaneous occurrence of two unrelated cytogenetic events. Am J Med Genet A (2007) 0.85
Molecular analysis of chromosome 7q21.3 in uterine leiomyoma: analysis using markers with linkage to insulin resistance. Cancer Genet Cytogenet (1998) 0.84
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study. J Med Genet (2006) 0.84
Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features. J Med Genet (1995) 0.84
Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors. Am J Med Genet (2002) 0.83
Small bowel obstruction in pregnancy. A review and report of four cases. Obstet Gynecol (1977) 0.83
An ultrasonic view of the developing fetus. Obstet Gynecol Surv (1983) 0.83
Mitogenic effect of basic fibroblast growth factor and estradiol on cultured human myometrial and leiomyoma cells. Am J Obstet Gynecol (1995) 0.82
Involvement of 10q22 in leiomyoma. Cancer Genet Cytogenet (1993) 0.82
Amniotic fluid catecholamines and metabolites in intrauterine growth retardation. Am J Obstet Gynecol (1981) 0.82
Grade 3 placentation: incidence and neonatal outcome. Obstet Gynecol (1983) 0.82
An ultrasonic view of the umbilical cord. Obstet Gynecol Surv (1987) 0.82
Combined laparoscopic and endoscopic excision of a gastric gist. Surg Endosc (2013) 0.81
Prenatal detection of congenital malformations by ultrasonography. Mayo Clinic experience. Am J Obstet Gynecol (1985) 0.81
Hydatidiform mole: parental chromosome aberrations in partial and complete moles. J Med Genet (1987) 0.81
Ultrasonic findings with holoprosencephaly. J Reprod Med (1982) 0.81
Nonsurgical management of placenta percreta: a case report. Obstet Gynecol (1994) 0.81
Amino acid sequence, post-translational modifications, binding and labelling of porcine odorant-binding protein. Chem Senses (1998) 0.80
An analysis of diabetic pregnancies at Mayo Clinic, 1950-79. Diabetes Care (1985) 0.80
Diagnosis and management of fetal distress. Mayo Clin Proc (1979) 0.80
Unusual presentations of fetal teratoma. J Perinatol (1991) 0.80
Evolving fetal hydranencephaly mimicking intracranial neoplasm. J Ultrasound Med (1991) 0.80
Genomic alterations in uterine leiomyosarcomas: potential markers for clinical diagnosis and prognosis. Genes Chromosomes Cancer (2001) 0.80
A sonographic and karyotypic study of second-trimester fetal choroid plexus cysts. Obstet Gynecol (1989) 0.79
Surgical drain after open or laparoscopic splenectomy: is it needed or contraindicated? G Chir (2015) 0.79
Severity of polyhydramnios does not affect the prevalence of large-for-gestational-age newborn infants. J Ultrasound Med (1996) 0.79
Comparison of magnesium sulfate, terbutaline and a placebo for inhibition of preterm labor. A randomized study. J Reprod Med (1984) 0.79
Cholecystectomy in pregnancy. Obstet Gynecol (1975) 0.79
Translocation (6;10)(p21;q22) in uterine leiomyomas. Cancer Genet Cytogenet (1995) 0.79
Clinical relevance of coagulation and renal changes in pre-eclampsia. Lancet (1978) 0.79
Purification, cloning and characterisation of odorant- and pheromone-binding proteins from pig nasal epithelium. Cell Mol Life Sci (2001) 0.79
Laparoscopic splenectomy in patients under the age of eighteen. Experience in 18 cases. G Chir (2011) 0.79
Terminal 2q deletion--a recognizable syndrome. Clin Genet (1997) 0.78
Polyp of the cecum. Laparoscopic-assisted polypectomy. G Chir (2012) 0.78
Ultrasonic evidence for luteinization of unruptured preovulatory follicles. Fertil Steril (1982) 0.78
Assessment of human follicular development of ultrasound. Mayo Clin Proc (1982) 0.78
Evaluation of three methods for estimating fetal weight. J Clin Ultrasound (1986) 0.78
Metabolism of uric acid in normal and toxemic pregnancy. Mayo Clin Proc (1978) 0.78
Ovarian surgery in pregnancy. Am J Obstet Gynecol (1975) 0.78
Subgroups of uterine leiomyomas based on cytogenetic analysis. Hum Pathol (1991) 0.78
Rearrangement of band 10q22 in leiomyoma and leiomyosarcoma of the uterus. Cancer Genet Cytogenet (1990) 0.78
Chromosome 7 biclonality in uterine leiomyoma. Cancer Genet Cytogenet (1993) 0.78
A hypervariable region at the D19S11 locus. Hum Genet (1987) 0.78
Fetal outcome after intraamniotic hemorrhage with placental abruption. A report of three cases. J Reprod Med (1986) 0.78
Laparoscopic-endoscopic rendez-vous resection of iuxta-cardial gastric GIST. G Chir (2013) 0.78
Deletion of chromosome 13 in leiomyomas of the uterus. Cancer Genet Cytogenet (1991) 0.78
The underlying cause of polyhydramnios determines prematurity. Prenat Diagn (1996) 0.78
Laparoscopic left colectomy: from the perfect knowledge of surgical anatomy to the proper surgical technique. G Chir (2010) 0.78
Average fetal depth in utero: data for estimation of fetal absorbed radiation dose. Radiology (1986) 0.78
Current uses of ultrasound in obstetrics. Prim Care (1983) 0.78
Sister chromatid exchange and chromosome breakage in complete hydatidiform moles. Cancer Genet Cytogenet (1992) 0.78
Bacterial expression and conformational analysis of a chemosensory protein from Schistocerca gregaria. Eur J Biochem (2001) 0.78
Cytogenetic analysis of a uterine lipoleiomyoma. Cancer Genet Cytogenet (1992) 0.78
Patient with partial mole requiring chemotherapy. Lancet (1978) 0.78