(Q33672396)

28 July 2017

Genetic analysis of malformations causing perinatal mortality (English)

1 reference

28 July 2017

Young ID

1

1 reference

28 July 2017

Rickett AB

series ordinal

2

1 reference

28 July 2017

Clarke M

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 February 1986

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

23

1 reference

28 July 2017

58-63

1 reference

28 July 2017

1

1 reference

The malformed fetus and stillbirth: whose patient?

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Perinatal mortality and neonatal survival in Avon: 1976-9.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Familial congenital diaphragmatic defects: aspects of etiology, prenatal diagnosis, and treatment

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Familial persistent pulmonary hypertension

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Confidential paediatric inquiry into neonatal deaths in Wessex, 1981 and 1982.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Quality of obstetric care provided for Asian immigrants in Leicestershire.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

The use of spontaneous abortuses and stillbirths in genetic counseling

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

High incidence of Meckel's syndrome in Gujarati Indians

21 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

21 June 2018

12 December 2020

Complex cardiac malformation in a case of trisomy 9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Holoprosencephaly: birth data, benetic and demographic analyses of 30 families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Syndromes of asplenia and polysplenia. A review of cardiac and non-cardiac malformations in 60 cases withspecial reference to diagnosis and prognosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

A family study of renal agenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

The Scottish perinatal mortality survey

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Evaluation of a protocol for post-mortem examination of stillbirths.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

The lethal multiple pterygium syndromes

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049543

The genetics of thanatophoric dwarfism

30 October 2018

1 reference

12 December 2020

Recurrence risks in a consecutive series of congenitally malformed children dying in the perinatal period

1 reference

12 December 2020

Chromosomes, syndromes, and perinatal deaths: the genetic counseling value of making a diagnosis in a malformed abortus, stillborn, and deceased newborn

1 reference

12 December 2020

Section II: diagnosis of the malformed abortus, stillborn, and deceased newborn--introductory remarks

1 reference

12 December 2020

Recurrence risk in osteogenesis imperfecta congenita

1 reference

12 December 2020

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses

1 reference

12 December 2020

Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration a european collaborative study on prenatal diagnoses 1981

1 reference

12 December 2020

Identifiers

PMCID

1049543

1 reference

28 July 2017

1 reference