Black SH - Search Results

1

Novel approach to the molecular diagnosis of Marfan syndrome: application to sporadic cases and in prenatal diagnosis.

Toudjarska I, Kilpatrick MW, Lembessis P, Carra S, Harton GL, Sisson ME, Black SH, Stern HJ, Gelman-Kohan Z, Shohat M, Tsipouras P. Toudjarska I, et al. Among authors: black sh. Am J Med Genet. 2001 Apr 1;99(4):294-302. doi: 10.1002/ajmg.1174. Am J Med Genet. 2001. PMID: 11251996

2

Preimplantation genetic diagnosis in Marfan syndrome.

Kilpatrick MW, Harton GL, Phylactou LA, Levinson G, Fugger EF, Schulman JD, Black SH, Tsipouras P. Kilpatrick MW, et al. Among authors: black sh. Fetal Diagn Ther. 1996 Nov-Dec;11(6):402-6. doi: 10.1159/000264355. Fetal Diagn Ther. 1996. PMID: 9115627

3

Preimplantation genetic testing for Marfan syndrome.

Harton GL, Tsipouras P, Sisson ME, Starr KM, Mahoney BS, Fugger EF, Schulman JD, Kilpatrick MW, Levinson G, Black SH. Harton GL, et al. Among authors: black sh. Mol Hum Reprod. 1996 Sep;2(9):713-5. doi: 10.1093/molehr/2.9.713. Mol Hum Reprod. 1996. PMID: 9239687

4

Improved sizing of fragile X CCG repeats by nested polymerase chain reaction.

Levinson G, Maddalena A, Palmer FT, Harton GL, Bick DP, Howard-Peebles PN, Black SH, Schulman JD. Levinson G, et al. Among authors: black sh. Am J Med Genet. 1994 Jul 15;51(4):527-34. doi: 10.1002/ajmg.1320510448. Am J Med Genet. 1994. PMID: 7943035

5

Non-disclosing preimplantation genetic diagnosis for Huntington disease.

Stern HJ, Harton GL, Sisson ME, Jones SL, Fallon LA, Thorsell LP, Getlinger ME, Black SH, Schulman JD. Stern HJ, et al. Among authors: black sh. Prenat Diagn. 2002 Jun;22(6):503-7. doi: 10.1002/pd.359. Prenat Diagn. 2002. PMID: 12116316

6

Preimplantation genetic diagnosis for spinal muscular atrophy type I.

Fallon L, Harton GL, Sisson ME, Rodriguez E, Field LK, Fugger EF, Geltinger M, Sun Y, Dorfmann A, Schoener C, Bick D, Schulman J, Levinson G, Black SH. Fallon L, et al. Among authors: black sh. Neurology. 1999 Sep 22;53(5):1087-90. doi: 10.1212/wnl.53.5.1087. Neurology. 1999. PMID: 10496271

7

Fragile X screening: what is the real issue?

Howard-Peebles PN, Maddalena A, Spence WC, Levinson G, Fallon L, Bick DP, Black SH, Schulman JD. Howard-Peebles PN, et al. Among authors: black sh. Am J Med Genet. 1994 Dec 1;53(4):382. doi: 10.1002/ajmg.1320530417. Am J Med Genet. 1994. PMID: 7864051 No abstract available.

8

Molecular fragile X screening in normal populations.

Spence WC, Black SH, Fallon L, Maddalena A, Cummings E, Menapace-Drew G, Bick DP, Levinson G, Schulman JD, Howard-Peebles PN. Spence WC, et al. Among authors: black sh. Am J Med Genet. 1996 Jul 12;64(1):181-3. doi: 10.1002/(SICI)1096-8628(19960712)64:1<181::AID-AJMG31>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8826471

9

Prenatal diagnosis of Sjögren-Larsson syndrome using enzymatic methods.

Rizzo WB, Craft DA, Kelson TL, Bonnefont JP, Saudubray JM, Schulman JD, Black SH, Tabsh K, Dirocco M, Gardner RJ. Rizzo WB, et al. Among authors: black sh. Prenat Diagn. 1994 Jul;14(7):577-81. doi: 10.1002/pd.1970140711. Prenat Diagn. 1994. PMID: 7971759

10

Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.

Cole H, Huang B, Salbert BA, Brown J, Howard-Peebles PN, Black SH, Dorfmann A, Febles OR, Stevens CA, Jackson-Cook C. Cole H, et al. Among authors: black sh. Am J Med Genet. 1994 Aug 15;52(2):136-45. doi: 10.1002/ajmg.1320520204. Am J Med Genet. 1994. PMID: 7801998 Review.

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