Schonberg S - Search Results

1

Recent experience in prenatal fra(X) detection.

Jenkins EC, Brown WT, Krawczun MS, Duncan CJ, Lele KP, Cantu ES, Schonberg S, Golbus MS, Sekhon GS, Stark S, et al. Jenkins EC, et al. Among authors: schonberg s. Am J Med Genet. 1988 May-Jun;30(1-2):329-36. doi: 10.1002/ajmg.1320300133. Am J Med Genet. 1988. PMID: 2972205

2

Prenatal detection of fra(X)(q27.3) in female identical twins: reliability of low level cytogenetic prenatal expression in females.

Jenkins EC, Brown WT, Schonberg S, Krawczun MS, Goldberg J, Golbus MS. Jenkins EC, et al. Among authors: schonberg s. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):128-35. doi: 10.1002/ajmg.1320430120. Am J Med Genet. 1992. PMID: 1605181

3

Transformation and establishment of fragile X cell lines from amniocytes.

Jenkins LS, Gruenert DC, Jenkins EC, Schonberg SA. Jenkins LS, et al. Among authors: schonberg sa. Am J Med Genet. 1991 Feb-Mar;38(2-3):416-7. doi: 10.1002/ajmg.1320380253. Am J Med Genet. 1991. PMID: 1850193

4

Application of flow karyotyping in prenatal detection of chromosome aberrations.

Gray JW, Trask B, van den Engh G, Silva A, Lozes C, Grell S, Schonberg S, Yu LC, Golbus MS. Gray JW, et al. Among authors: schonberg s. Am J Hum Genet. 1988 Jan;42(1):49-59. Am J Hum Genet. 1988. PMID: 3337112 Free PMC article.

5

Cytogenetic evidence for enhanced selective miscarriage of trisomy 21 pregnancies with advancing maternal age.

Kratzer PG, Golbus MS, Schonberg SA, Heilbron DC, Taylor RN. Kratzer PG, et al. Among authors: schonberg sa. Am J Med Genet. 1992 Nov 15;44(5):657-63. doi: 10.1002/ajmg.1320440526. Am J Med Genet. 1992. PMID: 1481829

6

Chorionic villus sampling: experience of the first 1000 cases.

Hogge WA, Schonberg SA, Golbus MS. Hogge WA, et al. Among authors: schonberg sa. Am J Obstet Gynecol. 1986 Jun;154(6):1249-52. doi: 10.1016/0002-9378(86)90707-6. Am J Obstet Gynecol. 1986. PMID: 3717235

7

Prenatal diagnosis by chorionic villus sampling: lessons of the first 600 cases.

Hogge WA, Schonberg SA, Golbus MS. Hogge WA, et al. Among authors: schonberg sa. Prenat Diagn. 1985 Nov-Dec;5(6):393-400. doi: 10.1002/pd.1970050605. Prenat Diagn. 1985. PMID: 4088973

8

Prenatal diagnosis of fragile (X) syndrome.

Hogge WA, Schonberg SA, Glover TW, Hecht F, Golbus MS. Hogge WA, et al. Among authors: schonberg sa. Obstet Gynecol. 1984 Mar;63(3 Suppl):19S-21S. Obstet Gynecol. 1984. PMID: 6700875

9

Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype.

Overhauser J, Golbus MS, Schonberg SA, Wasmuth JJ. Overhauser J, et al. Among authors: schonberg sa. Am J Hum Genet. 1986 Jul;39(1):1-10. Am J Hum Genet. 1986. PMID: 3752077 Free PMC article.

10

Mental retardation locus in Xp21 chromosome microdeletion.

Fries MH, Lebo RV, Schonberg SA, Golabi M, Seltzer WK, Gitelman SE, Golbus MS. Fries MH, et al. Among authors: schonberg sa. Am J Med Genet. 1993 Jun 1;46(4):363-8. doi: 10.1002/ajmg.1320460404. Am J Med Genet. 1993. PMID: 8357005

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