LillianY. F. Hsu

发表

Trisomy 8 mosaicism syndrome. Report of monozygotic twins

K. Hirschhorn, L. Hsu, J. Rose, 1978, Clinical genetics.

Prenatal diagnosis of 45,X/46,XY mosaicism with postnatal confirmation in a phenotypically normal male infant

K. Hirschhorn, L. Hsu, R. Hausknecht, 1976 .

Trisomy 20 mosaicism in prenatal diagnosis–a review and update

S. Kaffe, T. Perlis, L. Hsu, 1987, Prenatal diagnosis.

United states survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis

T. Perlis, L. Hsu, LillianY. F. Hsu, 1984, 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.

couples who have children with Down ' s syndrome , since their risk of recurrence is considerably greater than that of non-mosaic parent

Kurt, Hirschhorn, LillianY. F. Hsu, 2022 .

Prenatal diagnosis of genetic disease.

K. Hirschhorn, LillianY. F. Hsu, 1974, Advances in pathobiology.

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.

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.

Total finger ridge count and 45, X mosaicism (with and without Y chromosome)

K. Hirschhorn, LillianY. F. Hsu, J. M. Kerr, 1974, Clinical genetics.

Evidence for preferential involvement of chromosome bands 6p21 and 13q14 in amniotic fluid cell balanced translocation pseudomosaicism

L. Hsu, P. Benn, Peter A. Benn, 1986, Clinical genetics.

Trisomy 13 in bone marrow cells in acute myelocytic leukemia and myelofibrosis

M. Greenberg, L. Hsu, Simona Kohan, 1979, Clinical genetics.

Partial trisomy of the long arm of chromosome 1 in myelofibrosis and polycythemia vera

K. Hirschhorn, H. Gilbert, L. Hsu, 1977, American journal of hematology.

Revised guidelines for the diagnosis of mosaicism in amniocytes

P. Benn, LillianY. F. Hsu, 1999, Prenatal diagnosis.

A revisit of trisomy 20 mosaicism in prenatal diagnosis—an overview of 103 cases

S. Kaffe, T. Perlis, L. Hsu, 1991, Prenatal diagnosis.

Partial deletion of long arm of chromosome 11: del (11) (q23)

K. Hirschhorn, S. Kaffe, L. Hsu, 1977, Clinical genetics.

Familial chromosomal mosaicism, genetic aspects

K. Hirschhorn, M. Barcinski, L. Hsu, 1970 .

tri-Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome

LillianY. F. Hsu, FE PALo, Garcia, 2022 .

Trisomy 8 in bone marrow cells of patients with polycythemia vera and myelogenous leukemia

K. Hirschhorn, A. Alter, L. Hsu, 1974, Clinical Genetics.

ACQUIRED TRISOMIES 12 AND 7

K. Hirschhorn, S. Kaffe, C. Steer, 1974 .

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.