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Volumn 37, Issue 7, 2000, Pages
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Alstrom syndrome: confirmation of linkage to chromosome 2p12-13 and phenotypic heterogeneity in three affected sibs.
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
APOLIPOPROTEIN E;
ADOLESCENT;
BLOOD;
CHROMOSOME 2;
CONSANGUINITY;
FEMALE;
GENETIC HETEROGENEITY;
GENETIC LINKAGE;
GENETICS;
HUMAN;
HYPERCHOLESTEROLEMIA;
HYPERTRIGLYCERIDEMIA;
LETTER;
MALE;
NON INSULIN DEPENDENT DIABETES MELLITUS;
OBESITY;
PEDIGREE;
PERCEPTION DEAFNESS;
PHENOTYPE;
RETINITIS PIGMENTOSA;
SYNDROME;
ADOLESCENT;
APOLIPOPROTEINS E;
CHROMOSOMES, HUMAN, PAIR 2;
CONSANGUINITY;
DIABETES MELLITUS, TYPE 2;
FEMALE;
GENETIC HETEROGENEITY;
HEARING LOSS, SENSORINEURAL;
HUMANS;
HYPERCHOLESTEROLEMIA;
HYPERTRIGLYCERIDEMIA;
LOD SCORE;
MALE;
OBESITY;
PEDIGREE;
PHENOTYPE;
RETINITIS PIGMENTOSA;
SYNDROME;
MLCS;
MLOWN;
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EID: 0034221041
PISSN: None
EISSN: 14686244
Source Type: Journal
DOI: 10.1136/jmg.37.7.e8 Document Type: Letter |
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Times cited : (12)
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References (0)
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