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Annals of Human Genetics|March 27, 2023
Identification of pathogenic deep intronic variant and exonic LINE-1 insertion in a patient with Meckel syndromeSachiko Miyamoto, Kazuyuki Nakamura, Mitsuhiro Kato, et al.
Annals of Human Genetics|May 1, 1987
The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22M Azoulay, I Henry, F Tata, et al.
Annals of Human Genetics|May 1, 1985
Heritable fragile sites on human chromosomes. XII. Population cytogeneticsG R Sutherland
Annals of Human Genetics|July 1, 1985
Further studies on bivalent chiasma frequency in human males with normal karyotypesD A Laurie, M A Hultén
Annals of Human Genetics|July 1, 1985
Meiotic chromosome pairing in the normal human femaleB M Wallace, M A Hultén
Annals of Human Genetics|October 1, 1985
Use of robust variance components models to analyse triglyceride data in familiesT H Beaty, S G Self, K Y Liang, et al.
Annals of Human Genetics|November 8, 2012
Mutation detection in Croatian patients with familial hypercholesterolemiaIvan Pećin, Ros Whittall, Marta Futema, et al.
Annals of Human Genetics|October 1, 1988
A cytogenetic study of 47,XXY males of known origin and their parentsP A Jacobs, C Bacino, T Hassold, et al.
Annals of Human Genetics|October 1, 1988
Effects of environmental changes on the phenotypic expression of human polygenic traitsL Ulizzi, R Correani, L Terrenato
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