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The long arms of anencephaly: A refutation

Birth defects research. A Clinical and molecular teratology, 2009-08, Vol.85 (8), p.710-714

Barr Jr, Mason

2009

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M. Michael Cohen, Jr.: Author, diagnostician, geneticist, teacher, mentor, syndrome scholar extraordinaire (1937–2018)

American journal of medical genetics. Part A, 2018-08, Vol.176 (8), p.1703-1705

2018

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Prenatal diagnosis in pregnancies at risk for Joubert syndrome by ultrasound and MRI

Prenatal diagnosis, 2005-06, Vol.25 (6), p.442-447

2005

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Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome

Nature genetics, 2000-05, Vol.25 (1), p.79-82

2000

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Terminological inexactitude

American journal of medical genetics. Part A, 2007-12, Vol.143A (24), p.2886-2888

Barr, Jr, Mason

2007

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An updated history of the Teratology Society

Birth defects research. A Clinical and molecular teratology, 2010-05, Vol.88 (5), p.263-285

2010

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Familial 4;18 chromosome translocation resulting in trisomy 4p and monosomy 18p: affected individuals with discordant phenotype

Prenatal diagnosis, 2009-05, Vol.29 (5), p.538-540

2009

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Horseshoe adrenal gland in association with asplenia: presentation of six new cases and review of the literature

Pediatric radiology, 2002-11, Vol.32 (11), p.778-782

2002

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Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings

American journal of medical genetics. Part A, 2012-10, Vol.158A (10), p.2591-2601

2012

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Vascular steal: the pathogenetic mechanism producing sirenomelia and associated defects of the viscera and soft tissues

Pediatrics (Evanston), 1986-09, Vol.78 (3), p.451-457

1986

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Twin gestation: Influence of placentation on fetal growth

American journal of obstetrics and gynecology, 1991-10, Vol.165 (4), p.1394-1401

1991

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Renal tubular dysgenesis in twins

Pediatric nephrology (Berlin, West), 1998-06, Vol.12 (5), p.408-413

1998

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Cervical spine in the Apert syndrome

American journal of medical genetics, 1992-07, Vol.43 (4), p.704-708

1992

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Prenatal sonographic diagnosis of Nager acrofacial dysostosis with unilateral upper limb involvement

Prenatal diagnosis, 2008-10, Vol.28 (10), p.964-966

2008

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Angiotensin-converting enzyme inhibitor fetopathy

Journal of the American Society of Nephrology, 1993-03, Vol.3 (9), p.1575-1582

1993

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Holoprosencephaly in infants of diabetic mothers

The Journal of pediatrics, 1983-04, Vol.102 (4), p.565-568

1983

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Turner Syndrome morphology and morphometrics: Cardiac hypoplasia as a cause of midgestation death

Teratology (Philadelphia), 2002-08, Vol.66 (2), p.65-72

2002

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Autosomal recessive alobar holoprosencephaly with essentially normal faces

American journal of medical genetics, 2002-09, Vol.112 (1), p.28-30

2002

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Pitfall : anomalous umbilical vein and absent ductus venosus in association with right congenital diaphragmatic hernia

Pediatric radiology, 1997-08, Vol.27 (8), p.651-653

1997

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LOW-DOSE, SHORT-ACTING,ANGIOTENSIN-CONVERTING ENZYME INHIBITORS AS RESCUE THERAPY IN PREGNANCY

Obstetrics and gynecology (New York. 1953), 2001-05, Vol.97 (5), p.799

2001

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ACE inhibitor fetopathy and hypocalvaria: The kidney-skull connection

Teratology (Philadelphia), 1991-11, Vol.44 (5), p.485-495

1991

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Teratogen update: Angiotensin-converting enzyme inhibitors

Teratology (Philadelphia), 1994-12, Vol.50 (6), p.399-409

Barr Jr, Mason

1994

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Reply to Chudley

American journal of human genetics, 1991-07, Vol.49 (1), p.245-245

Barr, Mason

1991

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Holoprosencephaly survival and performance

American journal of medical genetics, 1999-06, Vol.89 (2), p.116-120

1999

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The long arms of anencephaly: A refutation

M. Michael Cohen, Jr.: Author, diagnostician, geneticist, teacher, mentor, syndrome scholar extraordinaire (1937–2018)

Prenatal diagnosis in pregnancies at risk for Joubert syndrome by ultrasound and MRI

Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome

Terminological inexactitude

An updated history of the Teratology Society

Familial 4;18 chromosome translocation resulting in trisomy 4p and monosomy 18p: affected individuals with discordant phenotype

Horseshoe adrenal gland in association with asplenia: presentation of six new cases and review of the literature

Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation

Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings

Vascular steal: the pathogenetic mechanism producing sirenomelia and associated defects of the viscera and soft tissues

Twin gestation: Influence of placentation on fetal growth

Renal tubular dysgenesis in twins

Cervical spine in the Apert syndrome

Prenatal sonographic diagnosis of Nager acrofacial dysostosis with unilateral upper limb involvement

Angiotensin-converting enzyme inhibitor fetopathy

Holoprosencephaly in infants of diabetic mothers

Turner Syndrome morphology and morphometrics: Cardiac hypoplasia as a cause of midgestation death

Autosomal recessive alobar holoprosencephaly with essentially normal faces

Pitfall : anomalous umbilical vein and absent ductus venosus in association with right congenital diaphragmatic hernia

LOW-DOSE, SHORT-ACTING,ANGIOTENSIN-CONVERTING ENZYME INHIBITORS AS RESCUE THERAPY IN PREGNANCY

ACE inhibitor fetopathy and hypocalvaria: The kidney-skull connection

Teratogen update: Angiotensin-converting enzyme inhibitors

Reply to Chudley

Holoprosencephaly survival and performance

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