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Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions.
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Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions.
Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions. Am J Hum Genet. 1997 May; 60(5):1184-93.
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PubMed
subject areas
Abnormalities, Multiple
Abnormalities, Multiple
Base Sequence
Base Sequence
Chromosome Banding
Chromosome Banding
Chromosome Inversion
Chromosome Inversion
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 17
Female
Female
Genetic Counseling
Genetic Counseling
Genotype
Genotype
Haplotypes
Haplotypes
Heterozygote
Heterozygote
Humans
Humans
In Situ Hybridization, Fluorescence
In Situ Hybridization, Fluorescence
Infant, Newborn
Infant, Newborn
Male
Male
Models, Genetic
Models, Genetic
Pedigree
Pedigree
Sequence Deletion
Sequence Deletion
Smith-Lemli-Opitz Syndrome
Smith-Lemli-Opitz Syndrome
authors with profiles
Sanjay I Bidichandani