L. Hsu

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Revised guidelines for the diagnosis of mosaicism in amniocytes

P. Benn, L. Hsu, L. Hsu, 1999, Prenatal diagnosis.

Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype–phenotype correlations

L. Shaffer, S. Patil, C. Jackson-Cook, 2000, Prenatal diagnosis.

Leukemia in Fanconi's anemia: cytogenetic and tumor virus susceptibility studies.

K. Hirschhorn, G. Todaro, Stanley L. Lee, 1970, Blood.

INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS: A COLLABORATIVE STUDY

B. Crandall, G. Stetten, J. Priest, 1996, Prenatal diagnosis.

Maternal serum alpha-fetoprotein screening and fetal chromosome anomalies: is lowering maternal age for amniocentesis preferable?

S. Kaffe, L. Hsu, 1992, American journal of medical genetics.

Prenatal Diagnosis of Chromosome Abnormalities

L. Hsu, 1986 .

Human chromosome identification by differential staining: G goup (21-22-Y).

K. Hirschhorn, L. Hsu, P. Chernay, 1971, Cytogenetics.

Cytogenetic studies in polycythemia vera.

B. Modan, K. Hirschhorn, J. Whang‐Peng, 1976, Seminars in hematology (Print).

Letter: Immunotherapy for colorectal cancer.

K Hirschhorn, K. Hirschhorn, L Y Hsu, 1976, Lancet.

The syndrome of ectrodactyly, ectodermal dysplasia and cleft lip and palate: report of a family demonstrating a dominant inheritance pattern

K. Hirschhorn, L. Hsu, C. Brill, 1972, Clinical genetics.

Prenatal diagnosis of 45,X/46,XY mosaicism—A review and update

L. Hsu, 1989, Prenatal diagnosis.

Numerical and Structural Chromosome Abnormalities

K. Hirschhorn, L. Hsu, 1977 .

Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.

L. Hsu, LillianY. F. Hsu, 1994, American journal of medical genetics.

Non-fluorescent and non-heterochromatic Y chromosome in 45, X 46,XY mosaicism.

L. Hsu, L. Steinfeld, H. J. Kim, 1974, Annales de genetique.

Problems in prenatal diagnosis resulting from chromosomal mosaicism

K. Hirschhorn, L. Hsu, N. Kardon, 1972, Clinical genetics.

Pitfalls in prenatal diagnosis resulting from chromosomal mosaicism.

K. Hirschhorn, L. Hsu, N. Kardon, 1972, The Journal of pediatrics.

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

K. Hirschhorn, A. Shanske, D. Warburton, 1992, Prenatal diagnosis.

Cytogenetic Aspects of Brain Dysfunction

K. Hirschhorn, L. Hsu, 1973 .

Trisomy 22: a clinical entity.

K. Hirschhorn, E. Lieber, L. Shapiro, 1971, The Journal of pediatrics.

Unusual Turner mosaicism (45,X-47,XXX;45,X-46,XXqi;45,X-46,XXr): detection through deceleration from mormal linear growth or secondary amenorrhea.

K. Hirschhorn, L. Hsu, 1971, The Journal of pediatrics.

Paternal trisomy 21 mosaicism and Down's syndrome.

K. Hirschhorn, L. Hsu, E. Leiter, 1971, American journal of human genetics.

Results and Pitfalls in Prenatal Cytogenetic Diagnosis

K. Hirschhorn, L. Hsu, T. Kerenyi, 1973, Journal of medical genetics.

Human chromosome identification by differential staining

K. Hirschhorn, L. Hsu, P. Chernay, 1971, Pediatric Research.

Meiosis in an XYY male.

K. Hirschhorn, L. Shapiro, L. Hsu, 1970, Lancet.

The centralized prenatal genetics screening program of New York City III: The first 7,000 cases.

P. Benn, L. Hsu, A. Carlson, 1985, American journal of medical genetics.

A fetus with a chromosome 13 ring and placenta with chromosome 13 rod/ring mosaicism

D. Warburton, J. Byrne, R. Rudelli, 1983, Prenatal diagnosis.

Neonatal Klinefelter's syndrome.

K. Hirschhorn, L. Shapiro, L. Hsu, 1969, American journal of diseases of children.

Prenatal cytogenetic diagnosis: first 1,000 successful cases.

K. Hirschhorn, L. Godmilow, S. Kaffe, 1978, American journal of medical genetics.

Prenatal diagnosis of double trisomy.

K. Hirschhorn, L. Strauss, A. Alter, 1975, American journal of diseases of children.

Section 2: Chromosome disease

A. Robinson, A. de la Chapelle, J. Hamerton, 1981 .

A rare case of 68,XX triploidy diagnosed by amniocentesis

S. Kaffe, N. Charles, L. Hsu, 1989, Prenatal diagnosis.

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

C L Bradshaw, L. Shaffer, C. Disteche, 1997, Prenatal diagnosis.

CHROMOSOME MOSAICISM AND PSEUDOMOSAICISM IN PRENATAL CYTOGENETIC DIAGNOSIS

T. Perlis, L. Hsu, 1982 .

Prenatal diagnosis of trisomy 20 mosaicism

E. Lieber, Jessica G. Davis, L. Hsu, 1979, Clinical genetics.

Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome

K. Hirschhorn, S. Kaffe, L. Hsu, 1974, Journal of medical genetics.

Fetal Wastage and Maternal Mosaicism

K. Hirschhorn, D. Grossman, L. Hsu, 1972, Obstetrics and gynecology.

Cytogenetics of fetal wastage.

K. Hirschhorn, L. Hsu, H. J. Kim, 1975, The New England journal of medicine.

A high incidence of maternal cell contamination of amniotic fluid cell cultures.

P. Benn, L. Hsu, A. Schonhaut, 1983, American journal of medical genetics.

A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres.

A. Henderson, D. Warburton, L. Shapiro, 1973, American journal of human genetics.

Prenatal diagnosis of genetic disease.

K. Hirschhorn, L. Hsu, 1974, Life sciences.

Stability of trisomic (47, 18+) cells in long-term mosaic skin fibroblast culture.

K. Hirschhorn, N. Beratis, L. Hsu, 1972, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

Incidence and significance of supernumerary marker chromosomes in prenatal diagnosis.

P. Benn, L. Hsu, 1984, American journal of human genetics.

Genetic and clinical considerations of long-arm deletion of the X chromosome.

K. Hirschhorn, L. Hsu, 1970, Pediatrics.

Klinefelter's syndrome in identical twins with the 46,XX chromosome constitution.

K. Hirschhorn, J. Gabrilove, G. Nicolis, 1972, The American journal of medicine.

A partial long arm deletion of chromosome 7:46,XY,del(7)(q32).

K. Hirschhorn, B. Kousseff, L. Hsu, 1977, Journal of medical genetics.

Prenatal Chromosome Analysis

K. Hirschhorn, L. Hsu, S. Cherry, 1970, Nature.

Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism

K. Hirschhorn, R. Moloshok, L. Hsu, 1978, Journal of medical genetics.

Chromosomal polymorphisms of 1, 9, 16, and Y in 4 major ethnic groups: a large prenatal study.

T. Perlis, P. Benn, L. Hsu, 1987, American journal of medical genetics.

A case of cri-du-chat associated with cataracts and transmitted from a mother with a 4-5 translocation.

K. Hirschhorn, L. Hsu, H. Grotsky, 1971, Journal of medical genetics.

Reciprocal translocation versus centric fusion between two No. 13 chromosomes. A case of 46,XX,-13,+t(13;13)(p12;q13) and a case of 46,XY,-13,+t(13;13)(p12;p12).

K. Hirschhorn, B. Kousseff, E. Sujansky, 1973, Cytogenetics and Cell Genetics.

Influence of Nuclear Selection Criteria on Sex Chromatin Frequency in Oral Mucosa Cells of Newborn Females

H. Klinger, L. Hsu, J. Weiss, 1967 .

Parental Chromosomal Aberrations Associated with Multiple Abortions and an Abnormal Infant

K. Hirschhorn, M. Barcinski, L. Shapiro, 1970, Obstetrics and gynecology.

THE 7p PARTIAL TRISOMY SYNDROME

K. Hirschhorn, J. Willner, L. Hsu, 1977, Pediatric Research.

Trisomy D in bone marrow cells in a patient with chronic myelogenous leukemia.

K. Hirschhorn, P. Papenhausen, M. Greenberg, 1974, Acta haematologica.

A differential staining technique for chromosome identification and its comparison with fluorescence technique

K. Hirschhorn, J. Kerr, N. Beratis, 1972, Clinical genetics.

Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.

K. Hirschhorn, L. Strauss, L. Hsu, 1977, Journal of medical genetics.

Pericentric inversion of the Y chromosome and prenatal diagnosis

D. Warburton, L. Shapiro, L. Hsu, 1984, Prenatal diagnosis.

The centralized prenatal genetics screening program of New York City: I. Developmental phase.

L. Hsu, 1981, American journal of medical genetics.

Parental mosaicism in trisomy 18.

K. Hirschhorn, N. Beratis, D. Grossman, 1972, Pediatrics.

Supernumerary small ring chromosome.

K. Hirschhorn, S. Kaffe, L. Hsu, 1977, Journal of medical genetics.

Supernumerary small ring chromosome ' SUMMARY

L. Hsu, H. J. Kim, Hirschhorn S Kaffe, 2022 .

XXXXY boy. A 15-month-old child with normal intellectual development.

K. Hirschhorn, L. Shapiro, L. Hsu, 1970, American journal of diseases of children.

Low X-chromatin frequency and frequency of inviable cells.

K. Hirschhorn, L. Hsu, 1972, Lancet.

Identification of Y and X Chromosomes in Amniotic Fluid Cells

K. Hirschhorn, L. Hsu, A. Rook, 1971, Nature.

The potential usefulness of computerized chromosome analysis in human genetics.

K. Hirschhorn, L. Hsu, 1972, Computers in biology and medicine.

Standardization in human cytogenetics

A. Chapelle, K. Hirschhorn, W. Sly, 1975 .

Deceleration of intellectual development in a XXXXY child: a follow-up.

K. Hirschhorn, L. Shapiro, L. Hsu, 1971, American journal of diseases of children.

Chromosome Abnormality in Offspring of LSD User: D Trisomy With D/D Translocation

K. Hirschhorn, L. Strauss, L. Hsu, 1970 .

47,XXY-48,XXXY-49,XXXXY mosaicism in a 4-year-old child.

K. Hirschhorn, N. Beratis, R. Moloshok, 1971, American journal of diseases of children.

Maternal cell contamination of amniotic fluid cell cultures: results of a U.S. nationwide survey.

P. Benn, L. Hsu, 1983, American journal of medical genetics.

Prenatal diagnosis of trisomy 18. Pathologic findings in 20-week conceptus.

K. Hirschhorn, L. Strauss, L. Hsu, 1973, American journal of diseases of children.

Pathologic Findings in 20-Week Conceptus

K. Hirschhorn, L. Strauss, L. Hsu, 2016 .

Prenatal diagnosis of 45,X/46,XY mosaicism—A review and update

L. Hsu, 1989 .

The use of amniocentesis for prenatal genetic counseling.

L. Hsu, K. Hirshhorn, M. Gertner, 1970, Bulletin of the New York Academy of Medicine.

ASSOCIATION OF 5q- AND REFRACTORY ANEMIA

K. Hirschhorn, R. Hoffman, S. Kaffe, 1977, Pediatric Research.

Cytogenetic findings in a parent of a patient with Fanconi's anemia

L. Spitler, H. Fudenberg, E. Lieber, 1972, Clinical genetics.

Sex chromosome mosaicism in 3 sibs

K. Hirschhorn, L. Hsu, H. Brendler, 1970 .