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Works matching IS 00034800 AND DT 2024 AND VI 88 AND IP 5

Results: 5

1

Attention‐deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2‐repeat allele.

Published in:

Annals of Human Genetics, 2024, v. 88, n. 5, p. 382, doi. 10.1111/ahg.12560

By:

Baum, Larry;
Lee, Chi Chiu;
Ye, Rui;
Zhong, Yuanxin;
Hung, Se Fong;
Tang, Chun Pan;
Ho, Ting Pong;
Swanson, James M;
Moyzis, Robert K;
Sham, Pak‐Chung;
Leung, Patrick Wing‐Leung

Publication type:

Article

2

Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia.

Published in:

Annals of Human Genetics, 2024, v. 88, n. 5, p. 364, doi. 10.1111/ahg.12559

By:

Almalki, Faisal

Publication type:

Article

3

NanoImprint: A DNA methylation tool for clinical interpretation and diagnosis of common imprinting disorders using nanopore long‐read sequencing.

Published in:

Annals of Human Genetics, 2024, v. 88, n. 5, p. 392, doi. 10.1111/ahg.12556

By:

Bækgaard, Caroline Hey;
Lester, Emilie Boye;
Møller‐Larsen, Steffen;
Lauridsen, Mathilde Faurholdt;
Larsen, Martin Jakob

Publication type:

Article

4

Using Drosophila amyloid toxicity models to study Alzheimer's disease.

Published in:

Annals of Human Genetics, 2024, v. 88, n. 5, p. 349, doi. 10.1111/ahg.12554

By:

Tsintzas, Elli;
Niccoli, Teresa

Publication type:

Article

5

Issue Information.

Published in:: Annals of Human Genetics, 2024, v. 88, n. 5, p. 1, doi. 10.1111/ahg.12516
Publication type:: Article