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Volume 49; Issue 2
Main
Human Heredity
Volume 49; Issue 2
Human Heredity
Volume 49; Issue 2
1
A Principal-Components Approach Based on Heritability for Combining Phenotype Information
Ott, Jü
,
rg
,
Rabinowitz, Daniel
Journal:
Human Heredity
Year:
1999
Language:
english
File:
PDF, 267 KB
Your tags:
english, 1999
2
Hereditary Desmoid Disease in a Family with a Germline Alu I Repeat Mutation of the APC Gene
Halling, Kevin C.
,
Lazzaro, Carlo R.
,
Honchel, Ronald
,
Bufill, José
,
A.
,
Powell, Steven M.
,
Arndt, Carola A.S.
,
Lindor, Noralane M.
Journal:
Human Heredity
Year:
1999
Language:
english
File:
PDF, 323 KB
Your tags:
english, 1999
3
Linkage Information Content of Polymorphic Genetic Markers
Guo, Xiuqing
,
Elston, RobertC.
Journal:
Human Heredity
Year:
1999
Language:
english
File:
PDF, 356 KB
Your tags:
english, 1999
4
Contribution of Interleukin 1β and KM Loci to Alopecia areata
Galbraith, GillianM.P.
,
Palesch, Yuko
,
Gore, ElizabethA.
,
Pandey, JanardanP.
Journal:
Human Heredity
Year:
1999
Language:
english
File:
PDF, 361 KB
Your tags:
english, 1999
5
Linkage information content of polymorphic genetic markers.
Guo, Xiuqing
,
Elston, Robert C
Journal:
Human Heredity
Year:
1999
Language:
english
File:
PDF, 377 KB
Your tags:
english, 1999
6
True Pedigree Errors More Frequent Than Apparent Errors for Single Nucleotide Polymorphisms
Gordon, Derek
,
Heath, SimonC.
,
Ott, Jürg
Journal:
Human Heredity
Year:
1999
Language:
english
File:
PDF, 296 KB
Your tags:
english, 1999
7
Analysis of the Complete Coding Region of the CFTR Gene in Ten Algerian Cystic Fibrosis Families
Loumi, O.
,
Baghriche, M.
,
Delpech, M.
,
Kaplan, J.C.
,
Bienvenu, T.
Journal:
Human Heredity
Year:
1999
Language:
english
File:
PDF, 226 KB
Your tags:
english, 1999
8
Human NDUFB9 Gene: Genomic Organization and a Possible Candidate Gene Associated with Deafness Disorder Mapped to Chromosome 8q13
Lin, Xin
,
Wells, Dan E.
,
Kimberling, William J.
,
Kumar, Shrawan
Journal:
Human Heredity
Year:
1999
Language:
english
File:
PDF, 377 KB
Your tags:
english, 1999
9
A Novel Splice Site Mutation in a Brazilian Patient with Hereditary Antithrombin Deficiency Type I
Arnaldi, LilianeA.T.
,
Polimeno, NewtonC.
,
Arruda, ValderR.
,
Annichino-Bizzacchi, JoyceM.
Journal:
Human Heredity
Year:
1999
File:
PDF, 184 KB
Your tags:
1999
10
A Novel Splice Site Mutation in a Brazilian Patient with Hereditary Antithrombin Deficiency Type I
Arnaldi, LilianeA.T.
,
Polimeno, NewtonC.
,
Arruda, ValderR.
,
Annichino-Bizzacchi, JoyceM.
Journal:
Human Heredity
Year:
1999
Language:
english
File:
PDF, 184 KB
Your tags:
english, 1999
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