Genetic counseling AND (genetic OR genomic) AND review - PubMed - NCBI

Genetic counseling AND (genetic OR genomic) AND review - PubMed - NCBI



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• PubMed links to genetics reviews articles for "Genetic counseling" 

Best matches for Genetic counseling AND (genetic OR genomic) AND review:

Genetic counselling, patient education, and informed decision-making in the genomic era.Metcalfe SA et al. Semin Fetal Neonatal Med. (2018)

Risk assessment, genetic counseling, and genetic testing for BRCA-related cancer in women: a systematic review to update the U.S. Preventive Services Task Force recommendation.Nelson HD et al. Ann Intern Med. (2014)

Missed therapeutic and prevention opportunities in women with BRCA-mutated epithelial ovarian cancer and their families due to low referral rates for genetic counseling and BRCA testing: A review of the literature.Hoskins PJ et al. CA Cancer J Clin. (2017)

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Select item 306114081.

Prenatal genetic testing and treatment for congenital adrenal hyperplasia.

Simpson JL, Rechitsky S.

Fertil Steril. 2019 Jan;111(1):21-23. doi: 10.1016/j.fertnstert.2018.11.041. Review.

PMID:

 

30611408

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Select item 306052972.

DYT-GNAL.

Deutschländer AB, Wszolek ZK.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews^®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2019 Jan 3.

PMID:

 

30605297

 

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Select item 306038073.

Pheochromocytoma and paraganglioma-an update on diagnosis, evaluation, and management.

Jain A, Baracco R, Kapur G.

Pediatr Nephrol. 2019 Jan 2. doi: 10.1007/s00467-018-4181-2. [Epub ahead of print] Review.

PMID:

 

30603807

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Select item 203014154.

Rothmund-Thomson Syndrome.

Wang LL, Plon SE.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews^®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
1999 Oct 6 [updated 2019 Jan 3].

PMID:

 

20301415

 

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Select item 305947325.

Lysosomal storage disorders affecting the heart: a review.

Nair V, Belanger EC, Veinot JP.

Cardiovasc Pathol. 2018 Dec 1;39:12-24. doi: 10.1016/j.carpath.2018.11.002. [Epub ahead of print] Review.

PMID:

 

30594732

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Select item 305922886.

Prenatal diagnosis of sex chromosome mosaicism with two marker chromosomes in three cell lines and a review of the literature.

Zheng J, Yang X, Lu H, Guan Y, Yang F, Xu M, Li M, Ji X, Wang Y, Hu P, Zhou Y.

Mol Med Rep. 2018 Dec 24. doi: 10.3892/mmr.2018.9798. [Epub ahead of print]

PMID:

 

30592288

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Select item 305848017.

Genetic predisposition to colorectal cancer: syndromes, genes, classification of genetic variants and implications for precision medicine.

Valle L, Vilar E, Tavtigian SV, Stoffel EM.

J Pathol. 2018 Dec 25. doi: 10.1002/path.5229. [Epub ahead of print] Review.

PMID:

 

30584801

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Select item 305738028.

Communication about genetic testing with breast and ovarian cancer patients: a scoping review.

Jacobs C, Patch C, Michie S.

Eur J Hum Genet. 2018 Dec 20. doi: 10.1038/s41431-018-0310-4. [Epub ahead of print] Review.

PMID:

 

30573802

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Select item 293695729.

TANGO2-Related Metabolic Encephalopathy and Arrhythmias.

Lalani SR, Graham B, Burrage L, Lai YC, Scaglia F, Soler-Alfonso C, Miyake C, Yang Y.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews^®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2018 Jan 25 [updated 2018 Dec 20].

PMID:

 

29369572

 

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Select item 3056694210.

Complex Small Supernumerary Marker Chromosome Leading to Partial 4q/21q Duplications: Clinical Implication and Review of the Literature.

Bellucco FT, Fock RA, de Oliveira-Júnior HR, Perez AB, Melaragno MI.

Cytogenet Genome Res. 2018 Dec 18. doi: 10.1159/000494682. [Epub ahead of print]

PMID:

 

30566942

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Select item 3056690411.

MANAGEMENT OF ENDOCRINE DISEASE: Diagnosis and management of the patient with non-classic CAH due to 21-hydroxylase deficiency.

Nordenstrom A, Falhammar H.

Eur J Endocrinol. 2018 Dec 1. pii: EJE-18-0712.R2. doi: 10.1530/EJE-18-0712. [Epub ahead of print] Review.

PMID:

 

30566904

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Select item 2030137312.

Hereditary Transthyretin Amyloidosis.

Sekijima Y.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews^®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2001 Nov 5 [updated 2018 Dec 20].

PMID:

 

20301373

 

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Select item 2030134013.

Alzheimer Disease Overview.

Bird TD.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews^®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
1998 Oct 23 [updated 2018 Dec 20].

PMID:

 

20301340

 

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Select item 2030130414.

Junctional Epidermolysis Bullosa.

Pfendner EG, Lucky AW.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews^®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2008 Feb 22 [updated 2018 Dec 20].

PMID:

 

20301304

 

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Select item 3055890315.

The role of genetic testing in dyslipidaemia.

Berberich AJ, Hegele RA.

Pathology. 2018 Dec 14. pii: S0031-3025(18)30502-6. doi: 10.1016/j.pathol.2018.10.014. [Epub ahead of print] Review.

PMID:

 

30558903

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Select item 3055865516.

Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype.

Lin PY, Tseng MH, Zenker M, Rao J, Hildebrandt F, Lin SH, Lin CC, Chang JH, Hsu CH, Lee MD, Lin SP, Tsai JD.

Orphanet J Rare Dis. 2018 Dec 17;13(1):226. doi: 10.1186/s13023-018-0961-9.

PMID:

 

30558655

 

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Select item 3055770217.

Measuring the economic value of genetic counselling.

Payne K, Eden M.

Eur J Med Genet. 2018 Dec 14. pii: S1769-7212(18)30547-0. doi: 10.1016/j.ejmg.2018.12.007. [Epub ahead of print] Review. No abstract available.

PMID:

 

30557702

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Select item 3055595718.

An update on the genetics of benign pituitary adenomas in children and adolescents.

Hannah-Shmouni F, Stratakis CA.

Curr Opin Endocr Metab Res. 2018 Aug;1:19-24. doi: 10.1016/j.coemr.2018.04.002. Epub 2018 Apr 24.

PMID:

 

30555957

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Select item 3055166519.

Pediatric Fatty Liver and Obesity: Not Always Justa Matter of Non-Alcoholic Fatty Liver Disease.

Alfani R, Vassallo E, De Anseris AG, Nazzaro L, D'Acunzo I, Porfito C, Mandato C, Vajro P.

Children (Basel). 2018 Dec 13;5(12). pii: E169. doi: 10.3390/children5120169. Review.

PMID:

 

30551665

 

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Select item 3054949520.

What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics.

Nurnberger JI Jr, Austin J, Berrettini WH, Besterman AD, DeLisi LE, Grice DE, Kennedy JL, Moreno-De-Luca D, Potash JB, Ross DA, Schulze TG, Zai G.

J Clin Psychiatry. 2018 Nov 27;80(1). pii: 17nr12046. doi: 10.4088/JCP.17nr12046.

PMID:

 

30549495

 

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