Malmgren H - Search Results

1

Molecular and clinical characterization of patients with overlapping 10p deletions.

Lindstrand A, Malmgren H, Verri A, Benetti E, Eriksson M, Nordgren A, Anderlid BM, Golovleva I, Schoumans J, Blennow E. Lindstrand A, et al. Among authors: malmgren h. Am J Med Genet A. 2010 May;152A(5):1233-43. doi: 10.1002/ajmg.a.33366. Am J Med Genet A. 2010. PMID: 20425828

2

Infantile autism--fragile X: molecular findings support genetic heterogeneity.

Malmgren H, Gustavson KH, Wahlström J, Arpi-Henriksson I, Bensch J, Pettersson U, Dahl N. Malmgren H, et al. Am J Med Genet. 1992 Dec 1;44(6):830-3. doi: 10.1002/ajmg.1320440624. Am J Med Genet. 1992. PMID: 1481857

3

Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers.

Iwarsson E, Malmgren H, Inzunza J, Ahrlund-Richter L, Sjöblom P, Rosenlund B, Fridström M, Hovatta O, Nordenskjöld M, Blennow E. Iwarsson E, et al. Among authors: malmgren h. Prenat Diagn. 2000 Dec;20(13):1038-47. Prenat Diagn. 2000. PMID: 11180227

4

Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalities.

Fridström M, Ahrlund-Richter L, Iwarsson E, Malmgren H, Inzunza J, Rosenlund B, Sjöblom P, Nordenskjöld M, Blennow E, Hovatta O. Fridström M, et al. Among authors: malmgren h. Prenat Diagn. 2001 Sep;21(9):781-7. doi: 10.1002/pd.173. Prenat Diagn. 2001. PMID: 11559915

5

Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrations.

Malmgren H, Sahlén S, Inzunza J, Aho M, Rosenlund B, Fridström M, Hovatta O, Ahrlund-Richter L, Nordenskjöld M, Blennow E. Malmgren H, et al. Mol Hum Reprod. 2002 May;8(5):502-10. doi: 10.1093/molehr/8.5.502. Mol Hum Reprod. 2002. PMID: 11994548

6

[Proposal for ethical guidelines concerning preimplantation genetic diagnosis].

Wahlström J, Blennow E, Nilsson L, Malmgren H, Munthe C, Westerholm B. Wahlström J, et al. Among authors: malmgren h. Lakartidningen. 2002 Mar 19;99(14):1568-73. Lakartidningen. 2002. PMID: 12025211 Swedish. No abstract available.

7

Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long-term cultivation.

Inzunza J, Sahlén S, Holmberg K, Strömberg AM, Teerijoki H, Blennow E, Hovatta O, Malmgren H. Inzunza J, et al. Among authors: malmgren h. Mol Hum Reprod. 2004 Jun;10(6):461-6. doi: 10.1093/molehr/gah051. Epub 2004 Mar 25. Mol Hum Reprod. 2004. PMID: 15044603

8

Molecular cytogenetic characterization of an insertional translocation, ins(6;7)(p25;q33q34): deletion/duplication of 7q33-34 and clinical correlations.

Malmgren H, Malm G, Sahlén S, Karlsson M, Blennow E. Malmgren H, et al. Am J Med Genet A. 2005 Nov 15;139(1):25-31. doi: 10.1002/ajmg.a.30983. Am J Med Genet A. 2005. PMID: 16222668

9

PGD for dystrophin gene deletions using fluorescence in situ hybridization.

Malmgren H, White I, Johansson S, Levkov L, Iwarsson E, Fridström M, Blennow E. Malmgren H, et al. Mol Hum Reprod. 2006 May;12(5):353-6. doi: 10.1093/molehr/gal039. Epub 2006 Apr 11. Mol Hum Reprod. 2006. PMID: 16608904

10

Distal 3p deletion syndrome: detailed molecular cytogenetic and clinical characterization of three small distal deletions and review.

Malmgren H, Sahlén S, Wide K, Lundvall M, Blennow E. Malmgren H, et al. Am J Med Genet A. 2007 Sep 15;143A(18):2143-9. doi: 10.1002/ajmg.a.31902. Am J Med Genet A. 2007. PMID: 17696125

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