Skip directly to search
Skip directly to A to Z list
Skip directly to navigation
Skip directly to page options
Skip directly to site content
Start of Search Controls
Search Form Controls
Search The CDC
submit
CDC A-Z Index
MENU
CDC A-Z
SEARCH
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
#
Search Form Controls
Search The CDC
submit
CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
About
Public Health Genomics Branch
PHGKB Weekly Horizon Scan
Genomics Precision Health Scan
Advanced Molecular Detection Clips
Non-Genomics Precision Health Scan
CDC-authored Publications Scan
Specialized PHGKB
Cancer PHGKB
Diabetes PHGKB
Economic Evaluation PHGKB
Environmental Health PHGKB
Family Health History PHGKB
Health Equity PHGKB
HLBS-PopOmics
Infectious Diseases PHGKB
Implementation Science PHGKB
Neurological Disorders PHGKB
Pharmacogenomics PHGKB
Primary Immune Deficiency Diseases PHGKB
Rare Diseases PHGKB
Reproductive and Child Health PHGKB
All Databases
COVID-19 GPH (47475)
CDC/NIH Web Information Database (32208)
CDC-Authored Genomics and Precision Health Publications Database (6094)
Precision Health Database (63881)
Tier-Classified Guidelines Database (535)
Pathogen Advanced Molecular Detection Database (26916)
All of Us Reports and Publications Database (698)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (227294)
Epigenetic Epidemiology Publications Database (22891)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Rare Diseases
Last data update: May 18, 2024
. (Total: 63881 Documents since 2012)
All
Cancer
Diabetes
Economic
Equity
Environmental
FHH
HLBS
ID
Implementation
ND
PGx
PI
Rare
RCH
dataset
All
GPH
Non-GPH
Filtered By
:
Select to fine-tune your search
Disease
Gene
Product Type
Category
Year
Previous
Records 1 - 12 (of 12 Records)
Query Trace:
Birt-Hogg-Dubé Syndrome and Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome: An Effective Multidisciplinary Approach to Hereditary Renal Cancer Predisposing Syndromes.
Al-Shinnag Mohammad et al. Frontiers in oncology 2021 11738822
Similar articles in PubMed
Colorectal cancer risk in families with Birt-Hogg-Dubé syndrome increased.
Sattler Elke C et al. European journal of cancer (Oxford, England : 1990) 2021 151168-174
Similar articles in PubMed
Structured assessment and followup for patients with hereditary kidney tumour syndromes.
Lattouf Jean-Baptiste et al. Canadian Urological Association journal = Journal de l'Association des urologues du Canada 10(7-8) E214-E222
Similar articles in PubMed
CLINGEN Actionability Report for Familial papillary renal cell carcinoma 1 - MET
ClinGen Actionability Working Group
CLINGEN Actionability Report for Birt-Hogg-Dub� syndrome - FLCN
ClinGen Actionability Working Group
Clinical and morphologic review of 60 hereditary renal tumors from 30 hereditary renal cell carcinoma syndrome patients: lessons from a contemporary single institution series.
Kennedy John M et al. Medical oncology (Northwood, London, England) 2019 Jul 36(9) 74
Similar articles in PubMed
The Relevance of Family History Taking in the Detection and Management of Birt-Hogg-Dubé Syndrome.
Torricelli Elena et al. Respiration; international review of thoracic diseases 2019 Jul 1-8
Similar articles in PubMed
Role of Radiologists in the Diagnosis of Unsuspected Birt-Hogg-Dubé Syndrome in a Tertiary Clinical Practice.
Lee Elizabeth et al. AJR. American journal of roentgenology 2019 May 1-6
Similar articles in PubMed
New Study Explains Why Genetic Mutations Cause Disease in Some People but Not in Others
Columbia Systems Biology News, August 2018
Hereditary renal cell carcinoma syndromes: diagnosis, surveillance and management.
Maher Eamonn R et al. World journal of urology 2018 Apr
Similar articles in PubMed
Birt-Hogg-Dubé syndrome: an underdiagnosed genetic tumor syndrome.
Steinlein Ortrud K et al. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 2018 Mar 16(3) 278-283
Similar articles in PubMed
A rapid NGS strategy for comprehensive molecular diagnosis of Birt-Hogg-Dubé syndrome in patients with primary spontaneous pneumothorax.
Zhang Xinxin et al. Respiratory research 2016 May 17(1) 64
Similar articles in PubMed
File Formats Help:
How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?
Adobe PDF file
Microsoft PowerPoint file
Microsoft Word file
Microsoft Excel file
Audio/Video file
Apple Quicktime file
RealPlayer file
Text file
Zip Archive file
SAS file
ePub file
Page last reviewed:
Feb 1, 2024
Page last updated:
May 18, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
TOP