Hirschhorn K - Search Results

1

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

Kaffe S, Hsu LY, Hirschhorn K. Kaffe S, et al. Among authors: hirschhorn k. J Med Genet. 1974 Dec;11(4):378-9. doi: 10.1136/jmg.11.4.378. J Med Genet. 1974. PMID: 4140911 Free PMC article.

2

Trisomy 8 mosaicism syndrome. Report of monozygotic twins.

Reyes PG, Hsu LY, Strauss L, Rose J, Hirschhorn K. Reyes PG, et al. Among authors: hirschhorn k. Clin Genet. 1978 Aug;14(2):90-7. doi: 10.1111/j.1399-0004.1978.tb02112.x. Clin Genet. 1978. PMID: 567548

3

Results and pitfalls in prenatal cytogenetic diagnosis.

Hsu LY, Dubin EC, Kerenyi T, Hirschhorn K. Hsu LY, et al. Among authors: hirschhorn k. J Med Genet. 1973 Jun;10(2):112-9. doi: 10.1136/jmg.10.2.112. J Med Genet. 1973. PMID: 4268389 Free PMC article.

4

Supernumerary small ring chromosome.

Kaffe S, Kim HJ, Hsu LY, Brill CB, Hirschhorn K. Kaffe S, et al. Among authors: hirschhorn k. J Med Genet. 1977 Dec;14(6):447-51. doi: 10.1136/jmg.14.6.447. J Med Genet. 1977. PMID: 604496 Free PMC article.

5

Prenatal diagnosis of 5p-.

David K, Kaffe S, Strauss L, Hsu LY, Serotkin A, Hirschhorn K. David K, et al. Among authors: hirschhorn k. Clin Genet. 1978 Feb;13(2):224-8. doi: 10.1111/j.1399-0004.1978.tb04253.x. Clin Genet. 1978. PMID: 627112

6

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

Hsu LY, Paciuc S, David K, Cristian S, Moloshok R, Hirschhorn K. Hsu LY, et al. Among authors: hirschhorn k. J Med Genet. 1978 Jun;15(3):222-6. doi: 10.1136/jmg.15.3.222. J Med Genet. 1978. PMID: 671488 Free PMC article.

7

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.

Kim HJ, Hsu LY, Goldsmith LC, Strauss L, Hirschhorn K. Kim HJ, et al. Among authors: hirschhorn k. J Med Genet. 1977 Apr;14(2):114-9. doi: 10.1136/jmg.14.2.114. J Med Genet. 1977. PMID: 853317 Free PMC article.

8

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

Hsu LY, Kim HJ, Hausknecht R, Hirschhorn K. Hsu LY, et al. Among authors: hirschhorn k. Clin Genet. 1976 Oct;10(4):232-8. doi: 10.1111/j.1399-0004.1976.tb00040.x. Clin Genet. 1976. PMID: 987872

9

Three successive prenatal diagnoses of 47,XY,+21.

Hsu LY, Godmilow L, Serotkiq AV, Hirschhorn K. Hsu LY, et al. Among authors: hirschhorn k. Clin Genet. 1976 Apr;9(4):412-6. doi: 10.1111/j.1399-0004.1976.tb02270.x. Clin Genet. 1976. PMID: 1261080

10

Problems in prenatal diagnosis resulting from chromosomal mosaicism.

Kardon NB, Chernay PR, Hsu LY, Martin JL, Hirschhorn K. Kardon NB, et al. Among authors: hirschhorn k. Clin Genet. 1972;3(2):83-9. doi: 10.1111/j.1399-0004.1972.tb01730.x. Clin Genet. 1972. PMID: 4115480 No abstract available.

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