Herva R - Search Results

1

Inherited interstitial del(Xp) with minimal clinical consequences: with a note on the location of genes controlling phenotypic features.

Herva R, Kaluzewski B, de la Chapelle A. Herva R, et al. Am J Med Genet. 1979;3(1):43-58. doi: 10.1002/ajmg.1320030110. Am J Med Genet. 1979. PMID: 474618

2

A large pericentric inversion of human chromosome 8.

Herva R, de la Chapelle A. Herva R, et al. Am J Hum Genet. 1976 May;28(3):208-12. Am J Hum Genet. 1976. PMID: 944528 Free PMC article.

3

Dicentric Y chromosome arising via tandem translocation.

Herva R, Saarinen I, Savikurki H, de la Chapelle A. Herva R, et al. Am J Med Genet. 1980;7(2):115-22. doi: 10.1002/ajmg.1320070205. Am J Med Genet. 1980. PMID: 7193412

4

A deletion in chromosome 22 can cause DiGeorge syndrome.

de la Chapelle A, Herva R, Koivisto M, Aula P. de la Chapelle A, et al. Among authors: herva r. Hum Genet. 1981;57(3):253-6. doi: 10.1007/BF00278938. Hum Genet. 1981. PMID: 7250965

5

Pericentric inversions of human chromosomes 9 and 10.

de la Chapelle A, Schröder J, Stenstrand K, Fellman J, Herva R, Saarni M, Anttolainen I, Tallila I, Tervilä L, Husa L, Tallqvist G, Robson EB, Cook PJ, Sanger R. de la Chapelle A, et al. Among authors: herva r. Am J Hum Genet. 1974 Nov;26(6):746-66. Am J Hum Genet. 1974. PMID: 4140690 Free PMC article. No abstract available.

6

Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene.

Aittomäki K, Herva R, Stenman UH, Juntunen K, Ylöstalo P, Hovatta O, de la Chapelle A. Aittomäki K, et al. Among authors: herva r. J Clin Endocrinol Metab. 1996 Oct;81(10):3722-6. doi: 10.1210/jcem.81.10.8855829. J Clin Endocrinol Metab. 1996. PMID: 8855829

7

The r(20) syndrome.

Herva R, Saarinen I, Leikkonen L. Herva R, et al. J Med Genet. 1977 Aug;14(4):281-3. doi: 10.1136/jmg.14.4.281. J Med Genet. 1977. PMID: 926142 Free PMC article.

8

Trisomy 9p with i(9p) and t(9q18p).

Herva R, Koivisto M. Herva R, et al. Hum Genet. 1979 Sep;50(3):237-40. doi: 10.1007/BF00399387. Hum Genet. 1979. PMID: 489006

9

Familial congenital diaphragmatic defects: aspects of etiology, prenatal diagnosis, and treatment.

Norio R, Kääriäinen H, Rapola J, Herva R, Kekomäki M. Norio R, et al. Among authors: herva r. Am J Med Genet. 1984 Feb;17(2):471-83. doi: 10.1002/ajmg.1320170210. Am J Med Genet. 1984. PMID: 6702899

10

Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals.

Mäkelä-Bengs P, Järvinen N, Vuopala K, Suomalainen A, Ignatius J, Sipilä M, Herva R, Palotie A, Peltonen L. Mäkelä-Bengs P, et al. Among authors: herva r. Am J Hum Genet. 1998 Aug;63(2):506-16. doi: 10.1086/301968. Am J Hum Genet. 1998. PMID: 9683599 Free PMC article.

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

149 results

Search Page