(Q41453510)

30 September 2017

1 reference

title

VACTERL-hydrocephaly, DK-phocomelia, and cerebro-cardio-radio-reno-rectal community (English)

1 reference

30 September 2017

Lurie IW

1

1 reference

30 September 2017

Ferencz C

series ordinal

2

1 reference

30 September 2017

publication date

1 May 1997

1 reference

American Journal of Medical Genetics Part A

30 September 2017

published in

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30 September 2017

volume

70

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30 September 2017

issue

2

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30 September 2017

page(s)

144-149

1 reference

Recurrence of diaphragmatic agenesis associated with multiple midline defects: evidence for an autosomal gene regulating the midline

30 September 2017

cites work

1 reference

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VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance

21 January 2018

1 reference

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VACTERL with hydrocephalus: further delineation of the syndrome(s)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Congenital abnormalities associated with limb deficiency defects: a population study based on cases from the Hungarian Congenital Malformation Registry (1975-1984).

21 January 2018

1 reference

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VACTERL with hydrocephalus and branchial arch defects: prenatal, clinical, and autopsy findings in two brothers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

VATER and hydrocephalus: distinct syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Aprosencephaly: review of the literature and report of a case with cerebellar hypoplasia, pigmented epithelial cyst and Rathke's cleft cyst

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

VACTERL plus hydrocephalus: A monogenic lethal condition

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Further delineation of the Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Occipital encephalocele and MURCS association: case report and review of central nervous system anomalies in MURCS patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomalies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Steinfeld syndrome: report of a second family and further delineation of a rare autosomal dominant disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

VACTERL or MURCS association in a girl with neurenteric cyst and identical thoracic malformations in the father: a case of gonosomal mosaicism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Walker-Warburg syndrome: report of three affected sibs

21 January 2018

1 reference

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Patterns in multimalformed babies and the question of the relationship between sirenomelia and VACTERL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

XK aprosencephaly and anencephaly in sibs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

DK-phocomelia syndrome in a child with a long follow-up

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

The Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Syndrome of multiple congenital malformations including phocomelia, thrombocytopenia, encephalocele, and urogenital abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Intrauterine Hydrocephalus and Ventriculomegaly: Associated Abnomalies and Fetal Outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

Baller-Gerold syndrome: a postmortem examination

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C144%3A%3AAID-AJMG8%3E3.0.CO%3B2-Y

10.1002/(SICI)1096-8628(19970516)70:2<144::AID-AJMG8>3.0.CO;2-Y

21 January 2018

Identifiers

DOI

1 reference

30 September 2017

1 reference