The genetic basis of female reproductive disorders: etiology and clinical testing
about
NELF knockout is associated with impaired pubertal development and subfertility.Genetic associations with diminished ovarian reserve: a systematic review of the literatureErythrocyte membrane antigen frequencies in patients with Type II congenital smell loss.A balanced chromosomal translocation involving chromosomes 3 and 16 in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome reveals new candidate genes at 3p22.3 and 16p13.3.The future for genetic studies in reproduction.The Genetics of Infertility: Current Status of the Field.Differential expression of nasal embryonic LHRH factor (NELF) variants in immortalized GnRH neuronal cell lines.In Vitro Activation: A Possible New Frontier for Treatment of Primary Ovarian Insufficiency.Physiological Aspects of Female Fertility: Role of the Environment, Modern Lifestyle, and Genetics.A genetic marker of the ACKR1 gene is present in patients with Type II congenital smell loss who have type I hyposmia and hypogeusia.Role of Oxidative Stress in Epigenetic Modification in Endometriosis.Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families.Polymorphism of Prophet of Pit-1 gene and its relationship with litter size of Small Tail Han sheep.Clinical genetic testing for Kallmann syndrome.Hypogonadotropic hypogonadism in a female patient previously diagnosed as having waardenburg syndrome due to a sox10 mutation.Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.
P2860
Q30359083-6B301488-0AEE-45D0-8330-D0804334C8CEQ34037220-2205E7B1-E076-412D-BE58-344306C12111Q35088269-74F3F837-17C0-4A60-BAE7-A6284BE2D7B9Q37140344-3794E090-1FA7-4179-A187-18F86F547A38Q37403131-8FB2D9AD-72A2-4503-8C4E-7035E59EFA9DQ37450892-F5F88E22-1A31-4C98-A3C2-2E49E7E861FCQ37595685-535ED6B0-C4C5-4C94-9880-717FF4217CFAQ38703453-F46EFBE8-797C-4E1F-BCB7-4D798739BE9DQ38851128-838ECC21-9F67-4625-B5C2-685918EFB67DQ39101877-D7B006FE-9696-4011-BFC1-3BF23951C8EFQ39263084-B94BB17C-CCA1-490B-9172-A9DC2875B66DQ40165512-2761538D-ED77-440D-B660-1B0AD3BE6815Q40746422-396DAAF6-9FC4-45FB-90DD-2DF2CFCE80EFQ43176450-7E6C9DD6-4E1C-4742-A950-21A0A4F351C9Q51109787-402E1156-E0D4-49DB-9661-8900817D3873Q52615329-4A2D7273-B729-4505-B4C5-1D4F225D0EB5
P2860
The genetic basis of female reproductive disorders: etiology and clinical testing
description
2013 nî lūn-bûn
@nan
2013 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
name
The genetic basis of female reproductive disorders: etiology and clinical testing
@ast
The genetic basis of female reproductive disorders: etiology and clinical testing
@en
The genetic basis of female reproductive disorders: etiology and clinical testing
@nl
type
label
The genetic basis of female reproductive disorders: etiology and clinical testing
@ast
The genetic basis of female reproductive disorders: etiology and clinical testing
@en
The genetic basis of female reproductive disorders: etiology and clinical testing
@nl
prefLabel
The genetic basis of female reproductive disorders: etiology and clinical testing
@ast
The genetic basis of female reproductive disorders: etiology and clinical testing
@en
The genetic basis of female reproductive disorders: etiology and clinical testing
@nl
P2860
P3181
P1476
The genetic basis of female reproductive disorders: etiology and clinical testing
@en
P2093
Lawrence C. Layman
P2860
P304
P3181
P356
10.1016/J.MCE.2013.02.016
P407
P577
2013-05-06T00:00:00Z