<--- Back to Details
First PageDocument Content
Propionic acidemia / Propionyl-CoA carboxylase / Genetic testing / Prenatal diagnosis / Health / Medicine / Rare diseases
Propionic acidemia
Propionyl-CoA carboxylase
Genetic testing
Prenatal diagnosis
Health
Medicine
Rare diseases

J Med Genet 1999;36:412–[removed]Short reports

Add to Reading List

Source URL: jmg.bmj.com

Download Document from Source Website

File Size: 184,90 KB

Share Document on Facebook

Similar Documents

TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD

TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD

DocID: 12v8A - View Document

Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee  draft findings

Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings

DocID: 12jOC - View Document

J Med Genet 1999;36:412–[removed]Short reports

J Med Genet 1999;36:412–[removed]Short reports

DocID: NHX0 - View Document

2013 General Session - Introduced Version - HB0145 - Insurance-coverage of phenylketonuria.

2013 General Session - Introduced Version - HB0145 - Insurance-coverage of phenylketonuria.

DocID: NC55 - View Document

2013 General Session - Engrossed Version - HB0145 - Insurance-coverage of inherited enzymatic disorders.

2013 General Session - Engrossed Version - HB0145 - Insurance-coverage of inherited enzymatic disorders.

DocID: NxPs - View Document