Blakemore K - Search Results

1

The utility of exome sequencing for fetal pleural effusions.

Jelin AC, Sobreira N, Wohler E, Solomon B, Sparks T, Sagaser KG, Forster KR, Miller J, Witmer PD, Hamosh A, Valle D, Blakemore K. Jelin AC, et al. Among authors: blakemore k. Prenat Diagn. 2020 Apr;40(5):590-595. doi: 10.1002/pd.5650. Epub 2020 Feb 17. Prenat Diagn. 2020. PMID: 31994743 Free PMC article.

2

Chorioangioma: a new inclusion in the prospective and retrospective evaluation of elevated maternal serum alpha-fetoprotein.

Thomas RL, Blakemore KJ. Thomas RL, et al. Among authors: blakemore kj. Prenat Diagn. 1990 Nov;10(11):691-6. doi: 10.1002/pd.1970101102. Prenat Diagn. 1990. PMID: 1704626

3

The vanishing twin: an explanation for discordance between chorionic villus karyotype and fetal phenotype.

Reddy KS, Petersen MB, Antonarakis SE, Blakemore KJ. Reddy KS, et al. Among authors: blakemore kj. Prenat Diagn. 1991 Sep;11(9):679-84. doi: 10.1002/pd.1970110903. Prenat Diagn. 1991. PMID: 1788173 Review.

4

The significance of trisomy 7 mosaicism in chorionic villus cultures.

Reddy KS, Blakemore KJ, Stetten G, Corson V. Reddy KS, et al. Among authors: blakemore kj. Prenat Diagn. 1990 Jul;10(7):417-23. doi: 10.1002/pd.1970100702. Prenat Diagn. 1990. PMID: 2235900

5

An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line.

Batista DA, Escallon C, Blakemore KJ, Stetten G. Batista DA, et al. Among authors: blakemore kj. Prenat Diagn. 1995 Feb;15(2):123-7. doi: 10.1002/pd.1970150203. Prenat Diagn. 1995. PMID: 7784362

6

Region-specific FISH probes used to identify and characterize an interstitial paracentric inv(21)(q22.1q22.3).

Torchia BS, Escallon C, Blakemore KJ, Stetten G. Torchia BS, et al. Among authors: blakemore kj. Prenat Diagn. 1998 Aug;18(8):849-53. Prenat Diagn. 1998. PMID: 9742577

7

Early second trimester prenatal diagnosis of Neu-Laxova syndrome.

Driggers RW, Isbister S, McShane C, Stone K, Blakemore K. Driggers RW, et al. Among authors: blakemore k. Prenat Diagn. 2002 Feb;22(2):118-20. doi: 10.1002/pd.228. Prenat Diagn. 2002. PMID: 11857616

8

Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation.

Cohn RD, Eklund E, Bergner AL, Casella JF, Woods SL, Althaus J, Blakemore KJ, Fox HE, Hoover-Fong JE, Hamosh A, Braverman NE, Freeze HH, Boyadjiev SA. Cohn RD, et al. Pediatrics. 2006 Aug;118(2):e514-21. doi: 10.1542/peds.2005-1307. Epub 2006 Jun 30. Pediatrics. 2006. PMID: 16816004

9

Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization.

Cain CC, Saul D, Attanasio L, Oehler E, Hamosh A, Blakemore K, Stetten G. Cain CC, et al. Among authors: blakemore k. Prenat Diagn. 2007 Apr;27(4):373-9. doi: 10.1002/pd.1674. Prenat Diagn. 2007. PMID: 17286317

10

Skeletal Dysplasias: Growing Therapy for Growing Bones.

Jelin AC, O'Hare E, Blakemore K, Jelin EB, Valle D, Hoover-Fong J. Jelin AC, et al. Among authors: blakemore k. Front Pharmacol. 2017 Mar 6;8:79. doi: 10.3389/fphar.2017.00079. eCollection 2017. Front Pharmacol. 2017. PMID: 28321190 Free PMC article. Review.

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