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Use of phenylalanine-to-tyrosine ratio determined by tandem mass spectrometry to improve newborn screening for phenylketonuria of early discharge specimens collected in the first 24 hours

Clinical chemistry (Baltimore, Md.), 1998-12, Vol.44 (12), p.2405-2409

1998

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Miscarriage risk from amniocentesis performed for abnormal maternal serum screening

American journal of obstetrics and gynecology, 2007-06, Vol.196 (6), p.608.e1-608.e5

2007

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The Absence of a Relation between the Periconceptional Use of Vitamins and Neural-Tube Defects

The New England journal of medicine, 1989-08, Vol.321 (7), p.430-435

1989

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The newborn screening educational gap: What prenatal care providers do compared with what is expected

American journal of obstetrics and gynecology, 2006, Vol.194 (1), p.131-137

2006

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Reducing the Need for Amniocentesis in Women 35 Years of Age or Older with Serum Markers for Screening

The New England journal of medicine, 1994-04, Vol.330 (16), p.1114-1118

1994

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Invasive Trophoblast Antigen (Hyperglycosylated Human Chorionic Gonadotropin) in Second-Trimester Maternal Urine as a Marker for Down Syndrome: Preliminary Results of an Observational Study on Fresh Samples

Clinical chemistry (Baltimore, Md.), 2004-01, Vol.50 (1), p.182-189

2004

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Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state

Genetic epidemiology, 1996, Vol.13 (5), p.501-512

1996

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Newborn screening: toward a uniform screening panel and system--executive summary

Pediatrics (Evanston), 2006-05, Vol.117 (5 Pt 2), p.S296-S307

2006

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Fetal growth and perinatal viability in California

Obstetrics and gynecology (New York. 1953), 1982-05, Vol.59 (5), p.624

1982

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Second-Trimester Maternal Serum Alpha-Fetoprotein Levels and the Risk of Subsequent Fetal Death

The New England journal of medicine, 1991-07, Vol.325 (1), p.6-10

1991

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Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss

Genetics in medicine, 2002-05, Vol.4 (3), p.162-171

2002

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Birth Prevalence of Primary Congenital Hypothyroidism by Sex and Ethnicity

Human biology, 1992-08, Vol.64 (4), p.531-538

1992

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Are obese women at higher risk for producing malformed offspring?

American journal of obstetrics and gynecology, 1994-02, Vol.170 (2), p.541-548

1994

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The association between maternal serum alpha-fetoprotein and preterm birth, small for gestational age infants, preeclampsia, and placental complications

Obstetrics and gynecology (New York. 1953), 1996-11, Vol.88 (5), p.816-822

1996

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Cost and effectiveness of the California triple marker prenatal screening program

Genetics in medicine, 1999-07, Vol.1 (5), p.199-206

1999

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Risk factors for congenital hypothyroidism: An investigation of infant's birth weight, ethnicity, and gender in California, 1990-1998

Teratology (Philadelphia), 2000-07, Vol.62 (1), p.36-41

2000

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Vitamin A and birth defects

American journal of obstetrics and gynecology, 1997-07, Vol.177 (1), p.31-36

1997

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Prenatal Genetic Services: Toward a National Data Base

Clinical obstetrics and gynecology, 1993-09, Vol.36 (3), p.510-520

1993

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Maternal Serum Alpha-fetoprotein Screening Activities of State Health Agencies: A Survey

Obstetrical & gynecological survey, 1991-07, Vol.46 (7), p.438-439

1991

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The genetics revolution: Ethical, legal, and insurance concerns

Postgraduate medicine, 2000-07, Vol.108 (1), p.193-202

Cunningham, George C.

2000

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Assessing number-specific error in the recall of onset of last menstrual period

Paediatric and perinatal epidemiology, 2000-07, Vol.14 (3), p.263-267

2000

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Newborn screening for sickle cell disease: 4 years of experience from California's newborn screening program

Journal of pediatric hematology/oncology, 1996-02, Vol.18 (1), p.36-41

1996

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Prenatal ultrasound findings in affected and unaffected pregnancies that are screen-positive for trisomy 18: the California experience

Prenatal diagnosis, 2000-04, Vol.20 (4), p.293-299

2000

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HOARDERS: CLEANING OUT THE CLIENT FILE CLUTTER

GP solo, 2012-07, Vol.29 (4), p.54-57

CUNNINGHAM, GEORGE C.

2012

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Reply to Lippman

American journal of human genetics, 1991-06, Vol.48 (6), p.1202-1202

Cunningham, George C.

1991

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Use of phenylalanine-to-tyrosine ratio determined by tandem mass spectrometry to improve newborn screening for phenylketonuria of early discharge specimens collected in the first 24 hours

Miscarriage risk from amniocentesis performed for abnormal maternal serum screening

The Absence of a Relation between the Periconceptional Use of Vitamins and Neural-Tube Defects

The newborn screening educational gap: What prenatal care providers do compared with what is expected

Reducing the Need for Amniocentesis in Women 35 Years of Age or Older with Serum Markers for Screening

Invasive Trophoblast Antigen (Hyperglycosylated Human Chorionic Gonadotropin) in Second-Trimester Maternal Urine as a Marker for Down Syndrome: Preliminary Results of an Observational Study on Fresh Samples

Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state

Newborn screening: toward a uniform screening panel and system--executive summary

Fetal growth and perinatal viability in California

Second-Trimester Maternal Serum Alpha-Fetoprotein Levels and the Risk of Subsequent Fetal Death

Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss

Birth Prevalence of Primary Congenital Hypothyroidism by Sex and Ethnicity

Are obese women at higher risk for producing malformed offspring?

The association between maternal serum alpha-fetoprotein and preterm birth, small for gestational age infants, preeclampsia, and placental complications

Cost and effectiveness of the California triple marker prenatal screening program

Risk factors for congenital hypothyroidism: An investigation of infant's birth weight, ethnicity, and gender in California, 1990-1998

Vitamin A and birth defects

Prenatal Genetic Services: Toward a National Data Base

Maternal Serum Alpha-fetoprotein Screening Activities of State Health Agencies: A Survey

The genetics revolution: Ethical, legal, and insurance concerns

Assessing number-specific error in the recall of onset of last menstrual period

Newborn screening for sickle cell disease: 4 years of experience from California's newborn screening program

Prenatal ultrasound findings in affected and unaffected pregnancies that are screen-positive for trisomy 18: the California experience

HOARDERS: CLEANING OUT THE CLIENT FILE CLUTTER

Reply to Lippman

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