(Q67694732)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

title

New chromosomal dysmorphic syndromes. 2. Trisomy 10p (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

author name string

S Stengel-Rutkowski

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

J D Murken

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

R Frankenberger

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

M Riechert

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

H Spiess

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

A Rodewald

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

J Stene

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

publication date

1 October 1977

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

17 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

volume

126

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

page(s)

109-125

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:913435%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00442193

17 September 2019

exact match

0 references

cites work

2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)

1 reference

12 December 2020

Observations with G bonding of human chromosomes. Reduction of dye concentration in Soerensen buffered solutions is sufficient for demonstrating G bands.

1 reference

12 December 2020

The dermatoglyphic pattern of the trisomy 10p syndrome

1 reference

12 December 2020

Precise identification of various chromosomal abnormalities.

1 reference

12 December 2020

Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).

1 reference

12 December 2020

"Cri du chat" syndrome with maternal insertional translocation

1 reference

12 December 2020

Del(10)p autosomal deletion syndrome: Clinical, cytogenetic and gene marker studies

1 reference

12 December 2020

Trisomy for the short arm of chromosome No. 10.

1 reference

12 December 2020

Exclusion gene mapping utilizing patients with chromosome imbalance: The HL-A system as a prototype

1 reference

12 December 2020

1 reference

12 December 2020

A case of multiple congenital anomalies with familial C-G translocation

1 reference

12 December 2020

Trisomy of the short arm of chromosome 10

1 reference

12 December 2020

1 reference

12 December 2020

Brother and sister with trisomy 10p: a new syndrome

1 reference

12 December 2020

MICROTECHNIQUE FOR CULTURING LEUKOCYTES FROM WHOLE BLOOD

1 reference

12 December 2020

Trisomy 10 p. A previously reported case explained by binding

1 reference

12 December 2020

Deletion of the short arm of chromosome No. 10.

1 reference

12 December 2020

An intersexual infant with an extra chromosome

1 reference

12 December 2020