Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13

1991 ◽  
Vol 87 (4) ◽  
Author(s):  
AnjanaLal Pettigrew ◽  
Frank Greenberg ◽  
C.Thomas Caskey ◽  
DavidH. Ledbetter
Keyword(s):  
Interstitial Deletion ◽  
Greig Syndrome

Interstitial deletion (2)(q11.2-q21) in a newborn with multiple malformations

2006 ◽  
Vol 37 (06) ◽  
Author(s):  
G Strobl-Wildemann ◽  
F Staudt ◽  
C Schmidtlein ◽  
U Heinrich
Keyword(s):  
Interstitial Deletion

A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum

1994 ◽  
Vol 3 (4) ◽  
pp. 296 ◽  
Author(s):  
M. GENUARDI ◽  
F. CALVIERI ◽  
C. TOZZI ◽  
R. COSLOVI ◽  
G. NERI
Keyword(s):  
Corpus Callosum ◽  
Interstitial Deletion

Interstitial deletion of the short arm of chromosome 3

1988 ◽  
Vol 79 (4) ◽  
Author(s):  
J.M. Hertz ◽  
W. Coerdt ◽  
N. Hahnemann ◽  
M. Schwartz
Keyword(s):  
Interstitial Deletion ◽  
Chromosome 3

Terminal or interstitial deletion in chromosome 8 long arm in Langer-Giedion syndrome (TRP II syndrome)?

1983 ◽  
Vol 64 (2) ◽  
pp. 163-166 ◽  
Author(s):  
Erica M. B�hler ◽  
U. K. B�hler ◽  
R. Christen
Keyword(s):  
Interstitial Deletion ◽  
Chromosome 8

scholarly journals A New Case of an Extremely Rare 3p21.31 Interstitial Deletion

2016 ◽  
Vol 7 (2) ◽  
pp. 93-98
Author(s):  
Luca Lovrecic ◽  
Sara Bertok ◽  
Mojca Žerjav Tanšek
Keyword(s):  
Interstitial Deletion

Interstitial deletion del(7)(q22;q31) in a case of Ph-negative CML

1985 ◽  
Vol 14 (1-2) ◽  
pp. 179-181 ◽  
Author(s):  
M.F. Turchini ◽  
A. Geneix ◽  
P. François ◽  
A. de Larocque ◽  
P. Malet
Keyword(s):  
Interstitial Deletion

Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies

1983 ◽  
Vol 64 (1) ◽  
pp. 97-97 ◽  
Author(s):  
P. Franceschini ◽  
M. Cirillo Silengo ◽  
G. Davi ◽  
R. Bianco ◽  
M. Biagioli
Keyword(s):  
Mental Retardation ◽  
Congenital Anomalies ◽  
Interstitial Deletion ◽  
Chromosome 3

First female prenatal case of osteopathia striata with cranial sclerosis in a fetus carrying a de-novo 1.9 Mbp interstitial deletion at Xq11.1q11.2

2017 ◽  
Vol 26 (4) ◽  
pp. 231-234
Author(s):  
Marie-Laure Vuillaume ◽  
Anna-Gaelle Valard ◽  
Nada Houcinat ◽  
Julie Bouron ◽  
Cécile Boucher ◽  
...  
Keyword(s):  
De Novo ◽  
Interstitial Deletion ◽  
Osteopathia Striata ◽  
Cranial Sclerosis
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