Haag MM - Search Results

1

Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome.

Rossbach HC, Sutcliffe MJ, Haag MM, Grana NH, Rossi AR, Barbosa JL. Rossbach HC, et al. Among authors: haag mm. Am J Med Genet. 1996 Jan 2;61(1):65-7. doi: 10.1002/(SICI)1096-8628(19960102)61:1<65::AID-AJMG12>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8741921

2

Recipient T-cell immune reconstitution in X-linked SCID after haploidentical maternal bone marrow transplant.

de la Morena MT, Wayne AS, Day NK, Haag MM, Hinds-Frey KR, Nelson RP, Sutcliffe MJ, Good RA. de la Morena MT, et al. Among authors: haag mm. Ann N Y Acad Sci. 1995 Dec 29;770:376-7. doi: 10.1111/j.1749-6632.1995.tb31074.x. Ann N Y Acad Sci. 1995. PMID: 8597380 No abstract available.

3

Pre-B acute lymphoblastic leukemia in a 3-year-old boy with pre-acute myelogenous leukemia myelodysplastic syndrome: cytogenetic evidence of common early progenitor cell ontogeny.

Rossbach HC, Sutcliffe MJ, Chamizo W, Haag MM, Grana NH, Washington KR, Barbosa JL. Rossbach HC, et al. Among authors: haag mm. J Pediatr Hematol Oncol. 1998 Jul-Aug;20(4):347-52. doi: 10.1097/00043426-199807000-00014. J Pediatr Hematol Oncol. 1998. PMID: 9703011

4

Clinicopathologic and genetic spectrum of infantile B-lymphoblastic leukemia: a multi-institutional study.

Knez V, Liu X, Schowinsky J, Pan Z, Wang D, Lorsbach R, Lu C, Luedke C, Haag M, Carstens B, Swisshelm K, Yang LH, Jug R, Wang E, Liang X. Knez V, et al. Leuk Lymphoma. 2019 Apr;60(4):1006-1013. doi: 10.1080/10428194.2018.1508667. Epub 2018 Sep 6. Leuk Lymphoma. 2019. PMID: 30188223

5

A multicenter analysis of individuals with a 47,XXY/46,XX karyotype.

Guess T, Wheeler FC, Yenamandra A, Schilit SLP, Anderson HS, Bone KM, Carstens B, Conlin L, Dulik MC, Dupont BR, Fanning E, Gardner JA, Haag M, Hilton BA, Johnson J, Kogan J, Murry J, Polonis K, Quigley DI, Repnikova EA, Rowsey RA, Spinner N, Stoeker M, Thurston V, Wiley M, Zhang L. Guess T, et al. Genet Med. 2024 Oct;26(10):101212. doi: 10.1016/j.gim.2024.101212. Epub 2024 Jul 14. Genet Med. 2024. PMID: 39011769

6

Clinical utility and cost-effectiveness analysis of chromosome testing concomitant with chromosomal microarray of patients with constitutional disorders in a U.S. academic medical center.

Su M, Page S, Haag M, Swisshelm K, Hennerich D, Graw S, LeRoux J, Brzeskiewicz P, Svihovec S, Bao L. Su M, et al. J Genet Couns. 2022 Apr;31(2):364-374. doi: 10.1002/jgc4.1496. Epub 2021 Aug 16. J Genet Couns. 2022. PMID: 34397147

7

21q22 amplification detection in three patients with acute myeloid leukemia: cytogenomic profiling and literature review.

Kudalkar EM, Pang C, Haag MM, Pollyea DA, Kamdar M, Xu G, Su M, Carstens B, Swisshelm K, Bao L. Kudalkar EM, et al. Among authors: haag mm. Mol Cytogenet. 2022 Jul 7;15(1):30. doi: 10.1186/s13039-022-00606-0. Mol Cytogenet. 2022. PMID: 35799207 Free PMC article.

8

'Deletion rescue' by mitotic 11q uniparental disomy in a family with recurrence of 11q deletion Jacobsen syndrome.

Johnson JP, Haag M, Beischel L, McCann C, Phillips S, Tunby M, Hansen J, Schwanke C, Reynolds JF. Johnson JP, et al. Clin Genet. 2014 Apr;85(4):376-80. doi: 10.1111/cge.12164. Epub 2013 May 28. Clin Genet. 2014. PMID: 23586500

9

Monozygosity by cell-free DNA screening in a dichorionic twin pregnancy with discordant fetal sex: Informed antenatal and postnatal care.

Porreco RP, Burson C, Bao L, Haag M. Porreco RP, et al. Prenat Diagn. 2020 May;40(6):758-760. doi: 10.1002/pd.5640. Epub 2020 Mar 3. Prenat Diagn. 2020. PMID: 31916615 No abstract available.

10

Cell-free DNA screening positive for monosomy X: clinical evaluation and management of suspected maternal or fetal Turner syndrome.

Dowlut-McElroy T, Davis S, Howell S, Gutmark-Little I, Bamba V, Prakash S, Patel S, Fadoju D, Vijayakanthi N, Haag M, Hennerich D, Dugoff L, Shankar RK. Dowlut-McElroy T, et al. Am J Obstet Gynecol. 2022 Dec;227(6):862-870. doi: 10.1016/j.ajog.2022.07.004. Epub 2022 Jul 13. Am J Obstet Gynecol. 2022. PMID: 35841934 Free PMC article.

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