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Beckwith–Wiedemann syndrome
Results: 23

#	Item
11	Folate-related genes and omphalocele Add to Reading List Source URL: www.health.ny.gov Language: English - Date: 2014-07-29 13:10:15 Dietary supplements Alcohols Methylenetetrahydrofolate reductase Folic acid Beckwith–Wiedemann syndrome Gastroschisis Omphalocele Neural tube defect Vitamin B12 Health Nutrition Biology
12	SHODAIR DNA LABORATORY TEST REQUEST FORM Add to Reading List Source URL: www.shodair.org Language: English - Date: 2013-12-05 14:18:06 Beckwith–Wiedemann syndrome Methylation Amniocentesis Thrombin Chemistry Biology Medicine
13	BREASTFEEDING MEDICINE Volume 1, Number 3, 2006 © Mary Ann Liebert, Inc. ABM Protocols ABM Clinical Protocol #1: Add to Reading List Source URL: www.bfmed.org Language: English - Date: 2012-02-16 15:41:18 Blood tests Health Hypoglycemia Blood sugar Beckwith–Wiedemann syndrome Breastfeeding Diabetes management Glucose test Blood glucose monitoring Diabetes Medicine Endocrine system
14	Microsoft Word - rcpu news - bws.doc Add to Reading List Source URL: www.peds.ufl.edu Language: English - Date: 2007-12-31 10:54:00 Beckwith–Wiedemann syndrome Medicine Health Biology
15	January,1990 #2.3 ALLIANCE ALERT Add to Reading List Source URL: www.geneticalliance.org Language: English - Date: 2013-07-25 16:12:11 Medical genetics Applied genetics Healthcare DNA Beckwith–Wiedemann syndrome Genetic counseling Genetic testing Health care provider DNA profiling Biology Medicine Genetics
16	Summer[removed]The Congenital Hyperinsulinism Center meet our TEAM Add to Reading List Source URL: www.chop.edu Language: English - Date: 2013-02-05 16:58:29 Congenital hyperinsulinism Hyperinsulinemic hypoglycemia Hypoglycemia Hyperinsulinism Diazoxide Kir6.2 Biology Beckwith–Wiedemann syndrome Idiopathic hypoglycemia Medicine Health Channelopathy
17	[removed]Genetics Evaluation, Referrals, and More—What To Do Next Carol L Greene, MD, FAAP, FACMG John B Moeschler, MD, MS, FAAP, FACMG Add to Reading List Source URL: www.geneticsinprimarycare.org Language: English - Date: 2013-03-12 11:54:32 Medical genetics Sotos syndrome Autism Triple X syndrome Perlman syndrome Beckwith–Wiedemann syndrome Hunter syndrome DiGeorge syndrome Marshall–Smith syndrome Health Syndromes Medicine
18	Time Out for Genetics Webinar Series Genetics Across the Lifespan–Putting it All Together While genetics is certainly crucial to human development over a life cycle, epigenetics, environmental factors and random event Add to Reading List Source URL: www.geneticsinprimarycare.org Language: English - Date: 2013-05-21 15:23:42 Medical genetics Fertility medicine Beckwith–Wiedemann syndrome Genetics Cystic fibrosis Genetic testing Genetic disorder Genetic counseling In vitro fertilisation Medicine Health Biology
19	Microsoft Word - OMPHALOCELE webprint.doc Add to Reading List Source URL: med.brown.edu Language: English - Date: 2009-03-24 14:57:45 Syndromes Gastroschisis Abdominal wall defect Pentalogy of Cantrell Pediatric surgery Beckwith–Wiedemann syndrome Cloacal exstrophy Patau syndrome Obstetrics Health Medicine Omphalocele
20	What is 22q11.2 Deletion Syndrome? 22q11.2 deletion syndrome is a genetic condition that affects learning, health, and physical traits. It occurs in males and females of all racial and ethnic backgrounds. 22q11.2 deletio Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 10:49:08 Marfan syndrome DiGeorge syndrome Angelman syndrome Down syndrome Genetic disorder Turner syndrome Noonan syndrome Genetic counseling Developmental disorder Health Syndromes Beckwith–Wiedemann syndrome

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