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X-chromosome abnormalities in women with premature ovarian failure

Journal of reproductive medicine, 1999-04, Vol.44 (4), p.321

1999

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Elevated second-trimester maternal serum hCG alone or in combination with elevated alpha-fetoprotein

Obstetrics and gynecology (New York. 1953), 1996-02, Vol.87 (2), p.217-222

1996

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Medians for second-trimester maternal serum α-fetoprotein, human chorionic gonadotropin, and unconjugated estriol; differences between races or ethnic groups

Clinical chemistry (Baltimore, Md.), 1997-02, Vol.43 (2), p.333-337

1997

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Down syndrome and neural tube defect screening: The value of using gestational age by ultrasonography

American journal of obstetrics and gynecology, 1997-05, Vol.176 (5), p.1056-1061

1997

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Evaluation of effect of analytical imprecision in maternal serum screening for Down's syndrome

Annals of clinical biochemistry, 2001-01, Vol.38 (Pt 1), p.28-36

2001

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45,X/46,XX mosaicism in patients with idiopathic premature ovarian failure

Fertility and sterility, 1998-07, Vol.70 (1), p.89-93

1998

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Prenatal diagnosis of diverse chromosome abnormalities in a population of patients identified by triple-marker testing as screen positive for Down syndrome

American journal of obstetrics and gynecology, 1995-08, Vol.173 (2), p.496-501

1995

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Maternal serum screening for fetal trisomy 18: a comparison of fixed cutoff and patient-specific risk protocols

Obstetrics and gynecology (New York. 1953), 1999-05, Vol.93 (5 Pt 1), p.707-711

1999

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Preliminary estimate for the second-trimester maternal serum screening detection rate of the 45,X karyotype using α-fetoprotein, unconjugated estriol and human chorionic gonadotropin

The journal of maternal-fetal & neonatal medicine, 2004-03, Vol.15 (3), p.160-166

2004

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Cost-effectiveness of estimating gestational age by ultrasonography in Down syndrome screening

Obstetrics and gynecology (New York. 1953), 1999-07, Vol.94 (1), p.29-33

1999

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Down syndrome and open neural tube defect screen-positive pregnancies: premature delivery and premature placental karyotyping

Prenatal diagnosis, 1997-03, Vol.17 (3), p.282-284

Benn, P A

1997

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Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies

Prenatal diagnosis, 1992-07, Vol.12 (7), p.555-573

1992

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RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS

Prenatal diagnosis, 1997-03, Vol.17 (3), p.201-242

1997

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Fine mapping of chromosome 22 breakpoints within the breakpoint cluster region (bcr) implies a role for bcr exon 3 in determining disease duration in chronic myeloid leukemia

American journal of human genetics, 1989-11, Vol.45 (5), p.729-738

1989

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Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin's lymphoma: results of the FAB LMB 96 international study

Leukemia, 2009-02, Vol.23 (2), p.323-331

2009

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Preliminary evidence for associations between second-trimester human chorionic gonadotropin and unconjugated oestriol levels with pregnancy outcome in Down syndrome pregnancies

Prenatal diagnosis, 1998-04, Vol.18 (4), p.319-324

Benn, Peter A.

1998

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Specific chromosome aberrations in senescent fibroblast cell lines derived from human embryos

American journal of human genetics, 1976-09, Vol.28 (5), p.465-473

Benn, P A

1976

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Estimates for the sensitivity and false-positive rates for second trimester serum screening for Down syndrome and trisomy 18 with adjustment for cross-identification and double-positive results

Prenatal diagnosis, 2001-01, Vol.21 (1), p.46-51

2001

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Incidence and significance of supernumerary marker chromosomes in prenatal diagnosis

American journal of human genetics, 1984-09, Vol.36 (5), p.1092-1102

1984

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Second trimester maternal serum analytes in triploid pregnancies: correlation with phenotype and sex chromosome complement

Prenatal diagnosis, 2001-08, Vol.21 (8), p.680-686

2001

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Altered Epidermal Growth Factor Signal Transduction in Activated Ha- ras-Transformed Human Keratinocytes

Biochemical and biophysical research communications, 1993-05, Vol.193 (1), p.167-174

1993

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Revised guidelines for the diagnosis of mosaicism in amniocytes

Prenatal diagnosis, 1999-11, Vol.19 (11), p.1081-1090

1999

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Role of ultrasound for Down syndrome screening in advanced maternal age

American journal of obstetrics and gynecology, 2001-11, Vol.185 (5), p.1028-1031

2001

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Densitometric analysis of southern blot autoradiographs and its application to monitoring patients with chronic myeloid leukemia

Leukemia, 1991-07, Vol.5 (7), p.540-547

1991

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Extreme second-trimester serum analyte values in Down syndrome pregnancies with hydrops fetalis

The journal of maternal-fetal & neonatal medicine, 2002, Vol.11 (4), p.262-265

2002

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X-chromosome abnormalities in women with premature ovarian failure

Elevated second-trimester maternal serum hCG alone or in combination with elevated alpha-fetoprotein

Medians for second-trimester maternal serum α-fetoprotein, human chorionic gonadotropin, and unconjugated estriol; differences between races or ethnic groups

Down syndrome and neural tube defect screening: The value of using gestational age by ultrasonography

Evaluation of effect of analytical imprecision in maternal serum screening for Down's syndrome

45,X/46,XX mosaicism in patients with idiopathic premature ovarian failure

Prenatal diagnosis of diverse chromosome abnormalities in a population of patients identified by triple-marker testing as screen positive for Down syndrome

Maternal serum screening for fetal trisomy 18: a comparison of fixed cutoff and patient-specific risk protocols

Preliminary estimate for the second-trimester maternal serum screening detection rate of the 45,X karyotype using α-fetoprotein, unconjugated estriol and human chorionic gonadotropin

Cost-effectiveness of estimating gestational age by ultrasonography in Down syndrome screening

Down syndrome and open neural tube defect screen-positive pregnancies: premature delivery and premature placental karyotyping

Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies

RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS

Fine mapping of chromosome 22 breakpoints within the breakpoint cluster region (bcr) implies a role for bcr exon 3 in determining disease duration in chronic myeloid leukemia

Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin's lymphoma: results of the FAB LMB 96 international study

Preliminary evidence for associations between second-trimester human chorionic gonadotropin and unconjugated oestriol levels with pregnancy outcome in Down syndrome pregnancies

Specific chromosome aberrations in senescent fibroblast cell lines derived from human embryos

Estimates for the sensitivity and false-positive rates for second trimester serum screening for Down syndrome and trisomy 18 with adjustment for cross-identification and double-positive results

Incidence and significance of supernumerary marker chromosomes in prenatal diagnosis

Second trimester maternal serum analytes in triploid pregnancies: correlation with phenotype and sex chromosome complement

Altered Epidermal Growth Factor Signal Transduction in Activated Ha- ras-Transformed Human Keratinocytes

Revised guidelines for the diagnosis of mosaicism in amniocytes

Role of ultrasound for Down syndrome screening in advanced maternal age

Densitometric analysis of southern blot autoradiographs and its application to monitoring patients with chronic myeloid leukemia

Extreme second-trimester serum analyte values in Down syndrome pregnancies with hydrops fetalis

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