Benn PA - Search Results

1

Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.

Delach JA, Rosengren SS, Kaplan L, Greenstein RM, Cassidy SB, Benn PA. Delach JA, et al. Among authors: benn pa. Am J Med Genet. 1994 Aug 1;52(1):85-91. doi: 10.1002/ajmg.1320520117. Am J Med Genet. 1994. PMID: 7977469

2

A rapid (but wrong) prenatal diagnosis.

Benn P, Ciarleglio L, Lettieri L, Rodis J, Greenstein R. Benn P, et al. N Engl J Med. 1992 Jun 11;326(24):1638-40. doi: 10.1056/nejm199206113262416. N Engl J Med. 1992. PMID: 1584278 No abstract available.

3

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

Benn PA, Horne D, Briganti S, Greenstein RM. Benn PA, et al. Am J Obstet Gynecol. 1995 Aug;173(2):496-501. doi: 10.1016/0002-9378(95)90272-4. Am J Obstet Gynecol. 1995. PMID: 7544068

4

Variable clinical expression of mosaic trisomy 16 in the newborn infant.

Devi AS, Velinov M, Kamath MV, Eisenfeld L, Neu R, Ciarleglio L, Greenstein R, Benn P. Devi AS, et al. Am J Med Genet. 1993 Aug 15;47(2):294-8. doi: 10.1002/ajmg.1320470231. Am J Med Genet. 1993. PMID: 8213923 Review.

5

Developing a role for genetics within a cancer program.

Pilarski RT, Greenstein RM, Benn P. Pilarski RT, et al. Ann N Y Acad Sci. 1995 Sep 30;768:258-60. doi: 10.1111/j.1749-6632.1995.tb12135.x. Ann N Y Acad Sci. 1995. PMID: 8526361 No abstract available.

6

Maternal serum screening for birth defects: results of a Connecticut regional program.

Benn PA, Horne D, Craffey A, Collins R, Ramsdell L, Greenstein R. Benn PA, et al. Conn Med. 1996 Jun;60(6):323-7. Conn Med. 1996. PMID: 8706425

7

Trisomy 16 mosaicism in amniotic fluid cell cultures.

Tantravahi U, Matsumoto C, Delach J, Craffey A, Smeltzer J, Benn P. Tantravahi U, et al. Prenat Diagn. 1996 Aug;16(8):749-54. doi: 10.1002/(SICI)1097-0223(199608)16:8<749::AID-PD935>3.0.CO;2-C. Prenat Diagn. 1996. PMID: 8878286

8

Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.

Cassidy SB, Forsythe M, Heeger S, Nicholls RD, Schork N, Benn P, Schwartz S. Cassidy SB, et al. Am J Med Genet. 1997 Feb 11;68(4):433-40. Am J Med Genet. 1997. PMID: 9021017

9

Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.

Greger V, Knoll JH, Wagstaff J, Woolf E, Lieske P, Glatt H, Benn PA, Rosengren SS, Lalande M. Greger V, et al. Among authors: benn pa. Am J Hum Genet. 1997 Mar;60(3):574-80. Am J Hum Genet. 1997. PMID: 9042916 Free PMC article.

10

Trisomy 16 and trisomy 16 Mosaicism: a review.

Benn P. Benn P. Am J Med Genet. 1998 Sep 1;79(2):121-33. Am J Med Genet. 1998. PMID: 9741470 Review.

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