Normal view MARC view ISBD view

A preliminary analysis of microplastics in edible versus non-edible tissues from seafood samples. [electronic resource]

By:

Akoueson, Fleurine

Contributor(s):

Producer: 20200710Description: 114452 p. digitalISSN:

1873-6424

Subject(s):

Online resources:

Available from publisher's website

In: Environmental pollution (Barking, Essex : 1987) vol. 263

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Journal Article

There are no comments on this title.

to post a comment.

Back to results

81 Isochromosome 5p, a novel recurrent abnormality in breast cancer: is it a common abnormality in cancer?
by Panani, Anna D
82 Isochromosomes 7q and 17q in Wilms tumor.
by Sreekantaiah, C
83 FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male.
by Codina-Pascual, M
84 Isoderivative chromosome 20 in bone marrow: three new cases.
by Shetty, Shashirekha
85 Origin of an apparent B chromosome by mutation, chromosome fragmentation and specific DNA sequence amplification.
by Dhar, Manoj K
86 Fetal facial profile in Pallister-Killian syndrome.
by Liberati, Marco
87 Isochromosome 17q in MDS: a marker of a distinct entity.
by Pinheiro, Ronald Feitosa
88 A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies.
by MacKinnon, Ruth N
89 The Turner syndrome life course project: Karyotype-phenotype analyses across the lifespan.
by Cameron-Pimblett, Antoinette
90 Prenatal diagnosis of isochromosome 20q in a fetus with vertebral anomaly and rocker-bottom feet.
by Receveur, Aline
91 Three patients with a 45,X/46,X,psu dic(Xp) karyotype.
by Dalton, P
92 Isochromosome 7q and Wilms tumor.
by Sandoval, C
93 TURNER SYNDROME DUE TO PRESUMPTIVE X-ISOCHROMOSOME; REPORT OF A CASE.
by SUMMITT, R L
94 Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies.
by Ligon, Azra H
95 Isochromosome i(17q) as a sole cytogenetic abnormality in a case of leukemic transformation from myelodysplastic syndrome (MDS)/myeloproliferative diseases (MPD).
by Nishida, Hiroko
96 45,X/46,X,i(Yp): Importance of Assessment and Support during Puberty and Adolescence.
by Gaudino, Rossella
97 Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma.
by Bettio, D
98 An uncommon complementary isochromosome of 46,XY, i(9)(p10),i(9)(q10) in an infertile oligoasthenoteratozoospermic man.
by Guvendag Guven, Emine Seda
99 [The medulloblastoma].
by Figols-Ladrón de Guevara, J
100 Isodicentric chromosome 21: a novel aberration in acute myeloid leukemia.
by Sankar, M