genereviews | GeneReviews®

Keyword	CPC	PCC	Volume	Score	Length of keyword
genereviews	1.68	0.7	2700	49	11

Keyword	CPC	PCC	Volume	Score
genereviews	1.5	0.9	2074	71
genereviews nf1	0.05	0.1	2451	58
genereviews pten	1.99	0.2	61	50
genereviews noonan	0.98	0.2	9867	45
genereviews vhl	0.72	0.2	5758	90
genereviews fabry	1.32	0.4	48	51
genereviews fragile x	0.37	0.6	6679	8
genereviews men1	1.17	0.6	8194	32
genereviews beckwith wiedemann	1.72	0.3	3133	72
genereviews tsc	1.76	0.4	1978	10
genereviews 22q11.2	1.92	0.2	9916	42
genereviews sma	1.56	0.1	4882	13
genereviews marfan	1.01	0.4	4907	20
genereviews ncbi	0.47	0.4	7975	90
genereviews dmd	0.95	0.5	3322	77
genereviews hht	0.11	0.1	4102	70
genereviews angelman	0.01	0.7	1023	60
genereviews prader willi	0.07	0.5	5718	56
genereviews myotonic dystrophy	1.59	0.6	6408	26
genereviews gtr	1.69	0.3	9942	18
genereviews cystic fibrosis	0.67	0.3	7536	40
genereviews turner syndrome	1.89	0.7	2106	6
genereviews japan	0.59	0.1	4679	66
genereviews marfan syndrome	1.56	0.1	1918	6
genereviews adpkd	0.13	0.5	7907	77

Search Results related to genereviews on Search Engine

GeneReviews® - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1116/

WEBSep 30, 2010 · GeneReviews, an international point-of-care resource for busy clinicians, provides clinically relevant and medically actionable information for inherited conditions in a standardized journal-style format, covering diagnosis, management, and genetic counseling for patients and their families.

DA: 96 PA: 20 MOZ Rank: 43

GeneReviews ® [Internet] - PubMed
nih.gov

https://pubmed.ncbi.nlm.nih.gov/20301295/

WEBGeneReviews, an international point-of-care resource for busy clinicians, provides clinically relevant and medically actionable information for inherited conditions in a standardized journal-style format, covering diagnosis, management, and genetic counseling for patients and their families.

DA: 92 PA: 3 MOZ Rank: 49

Cystic Fibrosis - GeneReviews® - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1250/

WEBMar 26, 2001 · Clinical Description. Cystic fibrosis (CF) affects the epithelia in several organs resulting in a complex, multisystem disease primarily involving the respiratory, gastrointestinal, genitourinary, and endocrine systems and the sweat glands.

DA: 24 PA: 65 MOZ Rank: 14

GeneReviews Glossary - GeneReviews® - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK5191/

WEBIn GeneReviews: referring to a disorder characterized by a constellation of phenotypic features that either: (1) specifically suggest the diagnosis (which can be confirmed by molecular genetic testing); or (2) allow diagnosis of the disorder in the absence of confirmatory molecular genetic findings. T targeted analysis for pathogenic variants

DA: 39 PA: 85 MOZ Rank: 42

GeneReviews - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/GeneReviews

WEBGeneReviews is an online database containing standardized peer-reviewed articles that describe specific heritable diseases. It was established in 1997 as GeneClinics by Roberta A Pagon (University of Washington) with funding from the National Institutes of Health.

DA: 72 PA: 54 MOZ Rank: 56

How well do you know GeneReviews®? - NCBI Insights
nih.gov

https://ncbiinsights.ncbi.nlm.nih.gov/2019/08/19/do-you-know-genereviews/

WEBAug 19, 2019 · You can volunteer to create a GeneReviews® chapter in your area of expertise. Start by reading the information for prospective authors. Our Educational Materials, designed for health care professionals of varying experience with clinical genetics, augment our glossary to clarify genetics concepts.

DA: 11 PA: 17 MOZ Rank: 66

GeneReviews – Genetics in Wisconsin – UW–Madison
wisc.edu

https://geneticsinwisconsin.wisc.edu/2021/07/23/genereviews/

WEBJul 23, 2021 · GeneReviews is an international point-of-care resource for busy clinicians, provides clinically relevant and medically actionable information for inherited conditions in a standardized journal-style format, covering diagnosis, management, and genetic counseling for patients and their families.

DA: 9 PA: 53 MOZ Rank: 8

Hereditary Paraganglioma-Pheochromocytoma Syndromes
nih.gov

https://pubmed.ncbi.nlm.nih.gov/20301715/

WEBSep 21, 2023 · Review. In: GeneReviews ® [Internet]. Seattle (WA): University of Washington, Seattle; 1993. 2008 May 21 [updated 2023 Sep 21]. Authors. Tobias Else 1 , Samantha Greenberg 2 , Lauren Fishbein 3. Book Editors. Margaret P Adam , Jerry Feldman , Ghayda M Mirzaa , Roberta A Pagon , Stephanie E Wallace , Lora JH Bean , …

DA: 37 PA: 71 MOZ Rank: 80

Multiple Endocrine Neoplasia Type 2 - GeneReviews® - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1257/

WEBSep 27, 1999 · Clinical characteristics. Multiple endocrine neoplasia type 2 (MEN2) includes the following phenotypes: MEN2A, familial medullary thyroid carcinoma (FMTC, which may be a variant of MEN2A), and MEN2B. All three phenotypes involve high risk for development of medullary carcinoma of the thyroid (MTC); MEN2A and MEN2B involve …

DA: 87 PA: 83 MOZ Rank: 35

Pseudocholinesterase deficiency: a comprehensive review of ... - PubMed
nih.gov

https://pubmed.ncbi.nlm.nih.gov/20879632/

WEBPseudocholinesterase deficiency is an inherited or acquired condition in which the metabolism of succinylcholine, mivacurium, or ester local anesthetics is potentially impaired. In this review, genetic inheritance, variants, and testing are examined.

DA: 5 PA: 25 MOZ Rank: 10