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Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancy

The Lancet (British edition), 1998-05, Vol.351 (9116), p.1624-1627

1998

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Mutations in SALL4 in malformed Father and Daughter postulated previously due to reflect mutagenesis by thalidomide

Birth defects research. A Clinical and molecular teratology, 2004-08, Vol.70 (8), p.550-551

2004

Volltextzugriff (PDF)

Increased rate of major malformations in offspring exposed to valproate during pregnancy

Neurology, 2005-03, Vol.64 (6), p.961

2005

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Guidelines for case classification for the national birth defects prevention study

Birth defects research. A Clinical and molecular teratology, 2003-03, Vol.67 (3), p.193-201

2003

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Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

Nature genetics, 1997-07, Vol.16 (3), p.311-315

1997

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Novel HOXA13 Mutations and the Phenotypic Spectrum of Hand-Foot-Genital Syndrome

American journal of human genetics, 2000-07, Vol.67 (1), p.197-202

2000

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Infants with Bochdalek diaphragmatic hernia: Sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program

American journal of medical genetics. Part A, 2005-10, Vol.138A (2), p.81-88

2005

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Heterotaxy: associated conditions and hospital-based prevalence in newborns

Genetics in medicine, 2000-05, Vol.2 (3), p.157-172

2000

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Absence/hypoplasia of tibia, polydactyly, retrocerebellar arachnoid cyst, and other anomalies: an autosomal recessive disorder

Journal of medical genetics, 1995-11, Vol.32 (11), p.896-900

1995

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Alcohol dehydrogenase 2 genotypes, maternal alcohol use, and infant outcome

The Journal of pediatrics, 2002-12, Vol.141 (6), p.780-785

2002

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The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human

The journal of clinical endocrinology and metabolism, 1996-12, Vol.81 (12), p.4388-4395

1996

Volltextzugriff (PDF)

Methodologic issues in epidemiologic studies of congenital microcephaly

Early human development, 2002-10, Vol.69 (1), p.91-105

2002

Volltextzugriff (PDF)

Putative new teratogens

Teratology (Philadelphia), 2002-05, Vol.65 (5), p.204-205

Holmes, Lewis B.

2002

Volltextzugriff (PDF)

A new syndrome: heart defects, laryngeal anomalies, preaxial polydactyly, and colonic aganglionosis in sibs

Genetics in medicine, 1999-03, Vol.1 (3), p.104-108

1999

Volltextzugriff (PDF)

Heterozygote advantage of the MTHFR gene in patients with neural-tube defect and their relatives

The Lancet (British edition), 1998-05, Vol.351 (9115), p.1554-1555

1998

Volltextzugriff (PDF)

Craniofacial skeletal deviations following in utero exposure to the anticonvulsant phenytoin: monotherapy and polytherapy

Orthodontics & craniofacial research, 2003-02, Vol.6 (1), p.2-19

2003

Volltextzugriff (PDF)

Possible fetal effects of cervical dilation and uterine curettage during the first trimester of pregnancy

The Journal of pediatrics, 1995, Vol.126 (1), p.131-134

Holmes, Lewis B.

1995

Volltextzugriff (PDF)

Contractures in a newborn infant of a mother with myasthenia gravis

The Journal of pediatrics, 1980-01, Vol.96 (6), p.1067-1069

1980

Volltextzugriff (PDF)

Teratogen-induced limb defects

American journal of medical genetics, 2002-10, Vol.112 (3), p.297-303

Holmes, Lewis B.

2002

Volltextzugriff (PDF)

Severe malformation of one foot from amniocentesis needle injury

Clinical dysmorphology, 1997-07, Vol.6 (3), p.273-280

Holmes, L B

1997

Volltextzugriff (PDF)

Adams-Oliver syndrome associated with cardiovascular malformations

Clinical dysmorphology, 1998-10, Vol.7 (4), p.235-241

1998

Volltextzugriff (PDF)

Prospective study showing that antisperm antibodies are not associated with pregnancy losses

Fertility and sterility, 1996-07, Vol.66 (1), p.36-42

1996

Volltextzugriff (PDF)

Issues in implementing prenatal screening for cystic fibrosis: results of a working conference

Genetics in medicine, 1999-05, Vol.1 (4), p.129-135

1999

Volltextzugriff (PDF)

Familial Nature of Congenital Absence and Severe Dysgenesis of Both Kidneys

The New England journal of medicine, 1984-05, Vol.310 (21), p.1341-1345

1984

Volltextzugriff (PDF)

Familial occurrence of malformations possibly attributable to vascular abnormalities

The Journal of pediatrics, 1986, Vol.108 (1), p.112-114

1986

Volltextzugriff (PDF)

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Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancy

Mutations in SALL4 in malformed Father and Daughter postulated previously due to reflect mutagenesis by thalidomide

Increased rate of major malformations in offspring exposed to valproate during pregnancy

Guidelines for case classification for the national birth defects prevention study

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

Novel HOXA13 Mutations and the Phenotypic Spectrum of Hand-Foot-Genital Syndrome

Infants with Bochdalek diaphragmatic hernia: Sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program

Heterotaxy: associated conditions and hospital-based prevalence in newborns

Absence/hypoplasia of tibia, polydactyly, retrocerebellar arachnoid cyst, and other anomalies: an autosomal recessive disorder

Alcohol dehydrogenase 2 genotypes, maternal alcohol use, and infant outcome

The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human

Methodologic issues in epidemiologic studies of congenital microcephaly

Putative new teratogens

A new syndrome: heart defects, laryngeal anomalies, preaxial polydactyly, and colonic aganglionosis in sibs

Heterozygote advantage of the MTHFR gene in patients with neural-tube defect and their relatives

Craniofacial skeletal deviations following in utero exposure to the anticonvulsant phenytoin: monotherapy and polytherapy

Possible fetal effects of cervical dilation and uterine curettage during the first trimester of pregnancy

Contractures in a newborn infant of a mother with myasthenia gravis

Teratogen-induced limb defects

Severe malformation of one foot from amniocentesis needle injury

Adams-Oliver syndrome associated with cardiovascular malformations

Prospective study showing that antisperm antibodies are not associated with pregnancy losses

Issues in implementing prenatal screening for cystic fibrosis: results of a working conference

Familial Nature of Congenital Absence and Severe Dysgenesis of Both Kidneys

Familial occurrence of malformations possibly attributable to vascular abnormalities

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