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Severe midline fusion defects in a newborn with 10q26----qter deletion.
Ann Genet. 1989; 32(2):124-5.AG

Abstract

In this report we describe a male newborn with a severe midline fusion syndrome associated with a "pure" distal 10q deletion (del(10)(q26.1----qter].

Authors+Show Affiliations

Centre for Human Genetics, U.Z. Gasthuisberg, Belgium.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

2757362

Citation

Fryns, J P., et al. "Severe Midline Fusion Defects in a Newborn With 10q26----qter Deletion." Annales De Genetique, vol. 32, no. 2, 1989, pp. 124-5.
Fryns JP, Kleczkowska A, Fivez H, et al. Severe midline fusion defects in a newborn with 10q26----qter deletion. Ann Genet. 1989;32(2):124-5.
Fryns, J. P., Kleczkowska, A., Fivez, H., & Van den Berghe, H. (1989). Severe midline fusion defects in a newborn with 10q26----qter deletion. Annales De Genetique, 32(2), 124-5.
Fryns JP, et al. Severe Midline Fusion Defects in a Newborn With 10q26----qter Deletion. Ann Genet. 1989;32(2):124-5. PubMed PMID: 2757362.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Severe midline fusion defects in a newborn with 10q26----qter deletion. AU - Fryns,J P, AU - Kleczkowska,A, AU - Fivez,H, AU - Van den Berghe,H, PY - 1989/1/1/pubmed PY - 1989/1/1/medline PY - 1989/1/1/entrez SP - 124 EP - 5 JF - Annales de genetique JO - Ann Genet VL - 32 IS - 2 N2 - In this report we describe a male newborn with a severe midline fusion syndrome associated with a "pure" distal 10q deletion (del(10)(q26.1----qter]. SN - 0003-3995 UR - https://www.unboundmedicine.com/medline/citation/2757362/Severe_midline_fusion_defects_in_a_newborn_with_10q26____qter_deletion_ DB - PRIME DP - Unbound Medicine ER -