PMID- 10577936
OWN - NLM
STAT- MEDLINE
DCOM- 20000127
LR  - 20181113
IS  - 0002-9297 (Print)
IS  - 0002-9297 (Linking)
VI  - 65
IP  - 6
DP  - 1999 Dec
TI  - Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome,
      Finnish type, in the old order Mennonites.
PG  - 1785-90
FAU - Bolk, S
AU  - Bolk S
FAU - Puffenberger, E G
AU  - Puffenberger EG
FAU - Hudson, J
AU  - Hudson J
FAU - Morton, D H
AU  - Morton DH
FAU - Chakravarti, A
AU  - Chakravarti A
LA  - eng
GR  - R01 HD028088/HD/NICHD NIH HHS/United States
GR  - R37 HD028088/HD/NICHD NIH HHS/United States
PT  - Letter
PL  - United States
TA  - Am J Hum Genet
JT  - American journal of human genetics
JID - 0370475
RN  - 0 (Membrane Proteins)
RN  - 0 (Proteins)
RN  - 0 (nephrin)
SB  - IM
MH  - Alleles
MH  - Child, Preschool
MH  - Christianity
MH  - Female
MH  - Finland
MH  - Gene Frequency/*genetics
MH  - *Genetic Heterogeneity
MH  - Haplotypes/genetics
MH  - Humans
MH  - Incidence
MH  - Infant
MH  - Linkage Disequilibrium/genetics
MH  - Male
MH  - Membrane Proteins
MH  - Mutation/genetics
MH  - Nephrotic Syndrome/*congenital/ethnology/*genetics
MH  - Pedigree
MH  - Pennsylvania/epidemiology
MH  - Proteins/genetics
PMC - PMC1288392
EDAT- 1999/12/01 09:00
MHDA- 2000/03/21 09:00
CRDT- 1999/12/01 09:00
PHST- 1999/12/01 09:00 [pubmed]
PHST- 2000/03/21 09:00 [medline]
PHST- 1999/12/01 09:00 [entrez]
AID - S0002-9297(07)63602-7 [pii]
AID - 10.1086/302687 [doi]
PST - ppublish
SO  - Am J Hum Genet. 1999 Dec;65(6):1785-90. doi: 10.1086/302687.