(Q42661138)

4 November 2017

Unknown syndrome: holoprosencephaly, congenital heart defects, and polydactyly (English)

1 reference

4 November 2017

0 references

1 reference

Young ID

1

1 reference

4 November 2017

Madders DJ

series ordinal

2

1 reference

4 November 2017

I D Young

series ordinal

1

0 references

D J Madders

series ordinal

2

0 references

language of work or name

English

0 references

publication date

1 November 1987

1 reference

Journal of Medical Genetics

4 November 2017

1 reference

4 November 2017

24

1 reference

4 November 2017

11

1 reference

4 November 2017

714-715

1 reference

The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patients.

4 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050355

PubMed Central

reference URL

A computerised data base for the diagnosis of rare dysmorphic syndromes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050355

PubMed Central

reference URL

Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly"

27 May 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/3430550

PubMed

reference URL

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.24.11.714

0 references

1 reference

4 November 2017

PubMed publication ID

3430550

1 reference