(Q44469307)

3 December 2017

Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome (English)

1 reference

3 December 2017

H J Lüdecke

1

1 reference

3 December 2017

R Burdiek

2

1 reference

3 December 2017

G Senger

3

1 reference

3 December 2017

U Claussen

4

1 reference

3 December 2017

E Passarge

5

1 reference

3 December 2017

B Horsthemke

6

1 reference

3 December 2017

1 July 1989

1 reference

3 December 2017

1 reference

3 December 2017

82

1 reference

3 December 2017

327-329

1 reference

3 December 2017

4

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00273991

3 December 2017

0 references

cites work

Langer-Giedion syndrome and additional congenital malformations with interstitial deletion of the long arm of chromosome 8 46, XY, del 8 (q 13-22)

1 reference

12 December 2020

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

12 December 2020

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?

1 reference

12 December 2020

Microdeletion syndromes, balanced translocations, and gene mapping

1 reference

12 December 2020

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

1 reference

12 December 2020

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors

1 reference

12 December 2020

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

12 December 2020

Homozygosity of chromosome 13 in retinoblastoma

1 reference

12 December 2020

Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients.

1 reference

12 December 2020

A final word on the tricho-rhino-phalangeal syndromes

1 reference

12 December 2020

Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus

1 reference

12 December 2020

Contiguous gene syndromes: a component of recognizable syndromes

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00273991

1 reference

3 December 2017

1 reference