Format
Items per page
Sort by

Send to:

Choose Destination

Results: 11

Related Articles by Review for PubMed (Select 9792866)

1.

Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37.

Visapää I, Fellman V, Varilo T, Palotie A, Raivio KO, Peltonen L.

Am J Hum Genet. 1998 Nov;63(5):1396-403.

2.

[GRACILE syndrome--a severe neonatal mitochondrial disorder].

Fellman V.

Duodecim. 2012;128(15):1560-7. Review. Finnish.

PMID:
22970607
3.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
4.

Meckel syndrome.

Salonen R, Paavola P.

J Med Genet. 1998 Jun;35(6):497-501. Review.

5.

Molecular background of the Finnish disease heritage.

Peltonen L.

Ann Med. 1997 Dec;29(6):553-6. Review.

PMID:
9562523
6.

Gene mapping of mineral metabolic disorders.

Thakker RV, Davies KE, O'Riordan JL.

J Inherit Metab Dis. 1989;12 Suppl 1:231-46. Review. Erratum in: J Inherit Metab Dis 1989;12(3):378.

PMID:
2681997
7.

Human genome organization of enzyme loci and metabolic diseases.

Shows TB.

Isozymes Curr Top Biol Med Res. 1983;10:323-39. Review. No abstract available.

PMID:
6354988
8.

Blau syndrome of granulomatous arthritis, iritis, and skin rash: a new family and review of the literature.

Manouvrier-Hanu S, Puech B, Piette F, Boute-Benejean O, Desbonnet A, Duquesnoy B, Farriaux JP.

Am J Med Genet. 1998 Mar 19;76(3):217-21. Review.

PMID:
9508240
9.

[Linkage and linkage disequilibrium in the Finnish disease heritage].

de la Chapelle A, Hästbacka J, Lehesjoki AE, Sulisalo T, Kere J, Tahvanainen E, Sistonen P.

Duodecim. 1994;110(7):654-64. Review. Finnish. No abstract available.

PMID:
8542820
10.

The Finnish disease heritage: a personal look.

Perheentupa J.

Acta Paediatr. 1995 Oct;84(10):1094-9. Review. No abstract available.

PMID:
8563216
11.

Metabolic liver disease in childhood.

Perlmutter DH.

Semin Gastrointest Dis. 1994 Apr;5(2):54-64. Review. No abstract available.

PMID:
8049907
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk