(Q41665551)

6 October 2017

Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome (English)

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

28 October 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1684953

chromosomal deletion syndrome

28 October 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1684953

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

28 October 2022

author name string

Scott CI Jr

4

1 reference

6 October 2017

J. E. Parrish

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1684953

28 October 2022

M. J. Wagner

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1684953

28 October 2022

J. T. Hecht

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1684953

28 October 2022

C. I. Scott

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1684953

28 October 2022

D. E. Wells

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1684953

28 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1684953

28 October 2022

publication date

1 September 1991

1 reference

full work available at URL

6 October 2017

https://api.elsevier.com/content/article/PII:088875439190101J?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

https://api.elsevier.com/content/article/PII:088875439190101J?httpAccept=text/plain

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

28 October 2022

1 reference

6 October 2017

11

1 reference

6 October 2017

1

1 reference

6 October 2017

54-61

1 reference

Homogeneously staining chromosomal regions contain amplified copies of an abundantly expressed cellular oncogene (c-myc) in malignant neuroendocrine cells from a human colon carcinoma

6 October 2017

1

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

The human thyroglobulin gene: A polymorphic marker localized distal to C-MYC on chromosome 8 band q24

28 October 2022

2

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

A final word on the tricho-rhino-phalangeal syndromes

28 October 2022

4

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

The tricho-rhino-phalangeal syndrome(s): chromosome 8 long arm deletion: is there a shortest region of overlap between reported cases? TRP I and TRP II syndromes: are they separate entities?

28 October 2022

5

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

A genetic linkage map of the human genome.

28 October 2022

8

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Isolation and analysis of the 21q+ chromosome in the acute myelogenous leukemia 8;21 translocation: evidence that c-mos is not translocated

28 October 2022

9

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

8q24.12 Interstitial deletion in trichorhinophalangeal syndrome type I

28 October 2022

10

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.

28 October 2022

11

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

trichorhinophalangeal syndrome type II

28 October 2022

12

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Assignment of the gene coding for phosphoribosylglycineamide formyltransferase to human chromosome 14.

28 October 2022

13

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

The tricho-rhino-phalangeal syndrome with exostoses (or Langer-Giedion syndrome): four additional patients without mental retardation and review of the literature

28 October 2022

14

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

cDNA isolation, expression analysis, and chromosomal localization of two human zinc finger genes

28 October 2022

15

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries

28 October 2022

16

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification

28 October 2022

17

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Partial trisomy of distal 8q derived from mother with mosaic 8q23.3----24.13 deletion, and relatively mild expression of trichorhinophalangeal syndrome I

28 October 2022

19

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

A routine method for the establishment of permanent growing lymphoblastoid cell lines

28 October 2022

20

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Langer-Giedion syndrome with del 8 (q24.13-q24.22)

28 October 2022

21

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Biochemical genetics of Chinese hamster cell mutants with deviant purine metabolism: isolation, selection, and characterization of a mutant lacking hypoxanthine-guanine phosphoribosyltransferase activity by nutritional means

28 October 2022

22

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Contiguous gene syndromes: a component of recognizable syndromes

28 October 2022

25

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Removal of repeated sequences from hybridisation probes

28 October 2022

26

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

A hybrid cell mapping panel for regional localization of probes to human chromosome 8

28 October 2022

28

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Human DNA sequence homologous to the transforming gene (mos) of Moloney murine sarcoma virus

28 October 2022

29

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

A DNA marker for human chromosome 8 that detects alleles of differing sizes

28 October 2022

30

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

Tricho-rhino-phalangeal syndrome type I with severe mental retardation due to interstitial deletion of 8q23.3-24.13.

28 October 2022

31

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

High Resolution of Human Chromosomes

28 October 2022

32

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90101-J

28 October 2022

Identifiers

1 reference

6 October 2017

1 reference