Mandahl N - Search Results

1

Trichorhinophalangeal syndrome type I: symptoms and signs, radiology and genetics.

Noltorp S, Kristoffersson UL, Mandahl N, Stigsson L, Svensson B, Werner CO. Noltorp S, et al. Among authors: mandahl n. Ann Rheum Dis. 1986 Jan;45(1):31-6. doi: 10.1136/ard.45.1.31. Ann Rheum Dis. 1986. PMID: 3954456 Free PMC article.

2

Normal high-resolution karyotypes in three patients with the Holt-Oram syndrome.

Kristoffersson U, Mineur A, Heim S, Mandahl N, Mitelman F. Kristoffersson U, et al. Among authors: mandahl n. Am J Med Genet. 1987 Sep;28(1):229-31. doi: 10.1002/ajmg.1320280135. Am J Med Genet. 1987. PMID: 3674114 No abstract available.

3

A squamous cell bladder carcinoma with karyotypic abnormalities reminiscent of transitional cell carcinoma.

Lundgren R, Elfving P, Heim S, Kristoffersson U, Mandahl N, Mitelman F. Lundgren R, et al. Among authors: mandahl n. J Urol. 1989 Aug;142(2 Pt 1):374-6. doi: 10.1016/s0022-5347(17)38765-7. J Urol. 1989. PMID: 2746756

4

Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, + i(8p)/46,XY.

Kristoffersson U, Lagergren J, Heim S, Mandahl N. Kristoffersson U, et al. Among authors: mandahl n. Clin Genet. 1988 Sep;34(3):201-3. doi: 10.1111/j.1399-0004.1988.tb02863.x. Clin Genet. 1988. PMID: 3180507

5

Increased frequency of chromosome aberrations in long-term cultured cerebrospinal fluid lymphocytes of patients with multiple sclerosis.

Sandberg-Wollheim M, Kristoffersson U, Mandahl N, Högstedt B. Sandberg-Wollheim M, et al. Among authors: mandahl n. J Neurol Sci. 1991 Mar;102(1):46-50. doi: 10.1016/0022-510x(91)90092-l. J Neurol Sci. 1991. PMID: 1856732

6

Structural chromosomal abnormalities of 3q in myelodysplastic syndrome/acute myeloid leukaemia with Sweet's syndrome.

Billström R, Heim S, Kristoffersson U, Mandahl N, Mitelman F. Billström R, et al. Among authors: mandahl n. Eur J Haematol. 1990 Sep;45(3):150-2. doi: 10.1111/j.1600-0609.1990.tb00442.x. Eur J Haematol. 1990. PMID: 2226727

7

Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemia.

Heim S, Kristoffersson U, Mandahl N, Malm C, Mitelman F. Heim S, et al. Among authors: mandahl n. Leukemia. 1988 Jan;2(1):65-7. Leukemia. 1988. PMID: 3422330

8

Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue.

Elfving P, Cigudosa JC, Lundgren R, Limon J, Mandahl N, Kristoffersson U, Heim S, Mitelman F. Elfving P, et al. Among authors: mandahl n. Cytogenet Cell Genet. 1990;53(2-3):123-5. doi: 10.1159/000132910. Cytogenet Cell Genet. 1990. PMID: 2369838

9

Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate.

Lundgren R, Kristoffersson U, Heim S, Mandahl N, Mitelman F. Lundgren R, et al. Among authors: mandahl n. Cancer Genet Cytogenet. 1988 Oct 1;35(1):103-8. doi: 10.1016/0165-4608(88)90128-8. Cancer Genet Cytogenet. 1988. PMID: 3180000

10

New structural chromosomal rearrangements in congenital leukemia.

Heim S, Békàssy AN, Garwicz S, Heldrup J, Wiebe T, Kristoffersson U, Mandahl N, Mitelman F. Heim S, et al. Among authors: mandahl n. Leukemia. 1987 Jan;1(1):16-23. Leukemia. 1987. PMID: 3312830 Review.

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