Anvret M - Search Results

1

[Preimplantation genetic diagnosis. An alternative to traditional prenatal diagnosis].

Iwarsson E, Blennow ES, Anvret M, Nordenskjöld M, Inzunza J, Ahrlund-Richter L, Pousette A, Hillensjó T, Fridström M, Rosenlund B, Sjöblom P. Iwarsson E, et al. Among authors: anvret m. Lakartidningen. 1997 Aug 27;94(35):2919-22. Lakartidningen. 1997. PMID: 9312603 Review. Swedish. No abstract available.

2

[The gene of spinal muscular atrophy localized. Possibilities for prenatal diagnosis].

Blennow ES, Bui TH, Söderhäll S, Anvret M, Nordenskjöld M. Blennow ES, et al. Among authors: anvret m. Lakartidningen. 1993 Jan 27;90(4):269-75. Lakartidningen. 1993. PMID: 8433608 Swedish. No abstract available.

3

Complex genetic counseling and exclusion of Duchenne muscular dystrophy in a twin pregnancy after in vitro fertilization (IVF).

Bui TH, Anvret M, Dahl N, Garoff L, Sjöblom P, Hillensjö T. Bui TH, et al. Among authors: anvret m. J Assist Reprod Genet. 1994 Mar;11(3):144-8. doi: 10.1007/BF02332091. J Assist Reprod Genet. 1994. PMID: 7827443

4

[Familial adenomatous polyposis. The gene of the disease was recently isolated--the pathogenesis of colonic cancer can be explained].

Hultcrantz R, Alm T, Anvret M, Nordenskjöld M. Hultcrantz R, et al. Among authors: anvret m. Lakartidningen. 1992 Oct 21;89(43):3593-5. Lakartidningen. 1992. PMID: 1334182 Review. Swedish. No abstract available.

5

[Diagnosis of cystic fibrosis by means of genetic technology--guidelines from an expert meeting].

Wahlström J, Annerén G, Anvret M, Bröndum-Nielsen K, Dahl N, Gustavson KH, Holmberg L, Holmgren G, Kollberg H, Kristoffersson U, et al. Wahlström J, et al. Among authors: anvret m. Lakartidningen. 1990 Oct 17;87(42):3429-30. Lakartidningen. 1990. PMID: 2233020 Swedish. No abstract available.

6

Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere.

Anvret M, Nordenskjöld M, Stolpe L, Johansson L, Bröndum-Nielsen K. Anvret M, et al. Hum Genet. 1991 Mar;86(5):481-3. doi: 10.1007/BF00194637. Hum Genet. 1991. PMID: 2016087

7

[Neuromuscular diseases. Molecular genetic methods will revolutionize diagnosis and treatment].

Anvret M, Edström L, Ahlberg G. Anvret M, et al. Lakartidningen. 1992 Mar 11;89(11):862, 865-9. Lakartidningen. 1992. PMID: 1545641 Review. Swedish. No abstract available.

8

[Development of molecular genetics and Charcot-Marie-Tooth disease. Important changes in clinical diagnostics].

Ericson U, Borg K, Anvret M. Ericson U, et al. Among authors: anvret m. Lakartidningen. 1997 Feb 5;94(6):428-30. Lakartidningen. 1997. PMID: 9053692 Review. Swedish. No abstract available.

9

[Diagnosis of cystic fibrosis with DNA techniques].

Anvret M, Dahl N. Anvret M, et al. Lakartidningen. 1991 Jan 30;88(5):316-7. Lakartidningen. 1991. PMID: 1997768 Swedish.

10

A normal male with an inherited deletion of one exon within the DMD gene.

Nordenskjöld M, Nicholson L, Edström L, Anvret M, Eiserman M, Slater C, Stolpe L. Nordenskjöld M, et al. Among authors: anvret m. Hum Genet. 1990 Jan;84(2):207-9. doi: 10.1007/BF00208944. Hum Genet. 1990. PMID: 2404853

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