Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.

Author:

Keppler-Noreuil K M,Carroll A J,Finley W H,Rutledge S L

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference6 articles.

1. Constitutional lp36 deletion in a child with neuroblastoma;Biegel, J.; White, P.S.; Marshall, H.N.;Am J Hum Genet,1993

2. chromosome 1 short arm in an infant with multiple anomalies: confirmation by in situ hybridization of probe p1-79;Magenis, R.E.; Sheehy, R.; Lacey, D.;Am J Hum Genet Suppl,1987

3. Partial monosomy of chromosome lp36. 3: a distinctive phenotype;AmJHum Genet Suppl,1994

4. Deletions (l)(p36.3) and the potential role of high resolution chromosome analysis;Wexler, P.; Gilfillan, T.; McGavran, L.; Sujansky, E.;Am Jf Hum Genet Suppl,1991

5. Yunis E, Quintero L, Leibovici M. Monosomy lpter. Hum Genet 1981;56:279-82.

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1. Monosomy 1p36: Report of a cohort of 13 Asian Indian patients;American Journal of Medical Genetics Part A;2022-01-06

2. Cardiovascular Phenotypic Spectrum of 1p36 Deletion Syndrome;Journal of Pediatric Genetics;2021-07-29

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

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