Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2017 1
2019 1
2024 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

3 results

Results by year

Filters applied: . Clear all
Page 1
Recent advances in trigonocephaly.
Mocquard C, Aillet S, Riffaud L. Mocquard C, et al. Neurochirurgie. 2019 Nov;65(5):246-251. doi: 10.1016/j.neuchi.2019.09.014. Epub 2019 Sep 27. Neurochirurgie. 2019. PMID: 31568780 Free article. Review.
Neurodevelopmental disorders are frequent in syndromic trigonocephaly and not particularly rare in non-syndromic cases (up to 34%). Developmental retardation (speech, motor or global) was almost always present in children exposed to valproic acid. Chromosomal …
Neurodevelopmental disorders are frequent in syndromic trigonocephaly and not particularly rare in non-syndromic cases (up to …
Genetics of human male infertility.
Poongothai J, Gopenath TS, Manonayaki S. Poongothai J, et al. Singapore Med J. 2009 Apr;50(4):336-47. Singapore Med J. 2009. PMID: 19421675 Free article. Review.
Each of these regions may be associated with a particular testicular histology, and several candidate genes have been found within these regions. The Deleted in Azoospermia (DAZ) gene family is reported to be the most frequently deleted AZF candidate gene …
Each of these regions may be associated with a particular testicular histology, and several candidate genes have been found within these reg …
[Usefulness of CGH-array and SNP-array for the etiological diagnosis of premature ovarian insufficiency].
Hyon C. Hyon C. Biol Aujourdhui. 2017;211(3):199-205. doi: 10.1051/jbio/2017025. Epub 2018 Feb 7. Biol Aujourdhui. 2017. PMID: 29412129 Review. French.
The karyotype allows to identify abnormalities of the number of chromosomes as well as abnormalities of the structure such as translocations, deletions or insertions of a size greater than 5-10 Mb Turner syndrome is the most frequent genetic cause of POI and …
The karyotype allows to identify abnormalities of the number of chromosomes as well as abnormalities of the structure such as translo …