de la Chapelle A - Search Results

1

[Current indications for chromosome study in congenital defects].

de la Chapelle A, Kääriäinen H, Salonen R. de la Chapelle A, et al. Duodecim. 1981;97(16):1320-32. Duodecim. 1981. PMID: 7327123 Finnish. No abstract available.

2

The MNSs blood groups of families with chromosome 4 rearrangements.

Cook PJ, Lindenbaum RH, Salonen R, de la Chapelle A, Daker MG, Buckton KE, Noades JE, Tippett P. Cook PJ, et al. Among authors: de la chapelle a. Ann Hum Genet. 1981 Feb;45(1):39-47. doi: 10.1111/j.1469-1809.1981.tb00304.x. Ann Hum Genet. 1981. PMID: 7316476 No abstract available.

3

Molecular mapping of the putative gonadoblastoma locus on the Y chromosome.

Salo P, Kääriäinen H, Petrovic V, Peltomäki P, Page DC, de la Chapelle A. Salo P, et al. Among authors: de la chapelle a. Genes Chromosomes Cancer. 1995 Nov;14(3):210-4. doi: 10.1002/gcc.2870140309. Genes Chromosomes Cancer. 1995. PMID: 8589038

4

Deletion mapping of stature determinants on the long arm of the Y chromosome.

Salo P, Kääriäinen H, Page DC, de la Chapelle A. Salo P, et al. Among authors: de la chapelle a. Hum Genet. 1995 Mar;95(3):283-6. doi: 10.1007/BF00225194. Hum Genet. 1995. PMID: 7868119

5

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

Sankila EM, Pakarinen L, Kääriäinen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A. Sankila EM, et al. Among authors: de la chapelle a. Hum Mol Genet. 1995 Jan;4(1):93-8. doi: 10.1093/hmg/4.1.93. Hum Mol Genet. 1995. PMID: 7711740

6

X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28.

Lehesjoki AE, Sankila EM, Miao J, Somer M, Salonen R, Rapola J, de la Chapelle A. Lehesjoki AE, et al. Among authors: de la chapelle a. J Med Genet. 1990 May;27(5):288-91. doi: 10.1136/jmg.27.5.288. J Med Genet. 1990. PMID: 1972196 Free PMC article.

7

Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.

Lindlöf M, Kääriäinen H, Davies KE, de la Chapelle A. Lindlöf M, et al. Among authors: de la chapelle a. J Med Genet. 1986 Dec;23(6):560-72. doi: 10.1136/jmg.23.6.560. J Med Genet. 1986. PMID: 2879928 Free PMC article.

8

Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations.

Lindlöf M, Kääriäinen H, van Ommen GJ, de la Chapelle A. Lindlöf M, et al. Among authors: de la chapelle a. Clin Genet. 1988 Feb;33(2):131-9. doi: 10.1111/j.1399-0004.1988.tb03424.x. Clin Genet. 1988. PMID: 3162851

9

Familial pericentric inversion inv(8)(p23q11).

Boyd H, Kaste J, Hovi E, Ritanen-Mohammed UM, Kääriäinen H, de la Chapelle A, Lehesjoki AE. Boyd H, et al. Among authors: de la chapelle a. J Med Genet. 1994 Mar;31(3):201-5. doi: 10.1136/jmg.31.3.201. J Med Genet. 1994. PMID: 8014967 Free PMC article.

10

Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.

Kääriäinen H, Lindlöf M, Somer H, de la Chapelle A. Kääriäinen H, et al. Among authors: de la chapelle a. Clin Genet. 1990 Mar;37(3):179-87. doi: 10.1111/j.1399-0004.1990.tb03500.x. Clin Genet. 1990. PMID: 1969777

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

668 results

Search Page