Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes-Reference-Cited by-同舟云学术

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Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes

Published:1999-01-29 Issue:3 Volume:82 Page:249-253
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Riegel Mariluce,Castellan Claudio,Balmer Damina,Brecevic Lukrecija,Schinzel Albert

Publisher

Wiley

Subject

Genetics (clinical)

Reference13 articles.

1. Monosomy 1p36.31–33→pter due to a paternal reciprocal translocation: Prognostic significance of FISH analysis

2. Prenatal diagnosis in CDG1 families: beware of heterogeneity

3. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

4. Molecular-cytogenetic detection of a deletion of 1p36.3.

5. AN INTERSTITIAL TRANSLOCATION: CHROMOSOME NO. 1p TO 4q

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1. Human Genetics of Ebstein Anomaly;Advances in Experimental Medicine and Biology;2024

2. Outcome of Vertical Expandable Prosthetic Titanium Rib (VEPTR) Instrumentation in Scoliosis Associated With 1p36 Deletion Syndrome: A Case Report;Cureus;2022-01-23

3. DELETION 1p36 SYNDROME;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

4. Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review;Epilepsy Research;2018-01

5. Identification of a New Candidate Locus for Ebstein Anomaly in 1p36.2;Molecular Syndromology;2018

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