N V Rumyantseva
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Explore the profile of N V Rumyantseva including associated specialties, affiliations and a list of published articles.
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4
Citations
33
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Recent Articles
1.
Barber J, Zhang S, Friend N, Collins A, Maloney V, Hastings R, et al.
Cytogenet Genome Res
. 2006 Sep;
114(3-4):351-8.
PMID: 16954678
Extra euchromatic material was found within the major heterochromatic block of chromosome 16 (16qh) in one de novo case and seven members of two families. In contrast to the euchromatic...
2.
Lin A, GORLIN R, Lurie I, Brunner H, van der Burgt I, Naumchik I, et al.
Am J Med Genet
. 1995 Mar;
56(1):42-59.
PMID: 7747785
We review 43 patients (15 new, 28 literature) with the branchio-oculo-facial (BOF) syndrome, which has a distinctive phenotype ranging from mild to severe forms, consisting of eye, ear, oral, and...
3.
Lurie I, Ilyina H, Gurevich D, Rumyantseva N, Naumchik I, Castellan C, et al.
Am J Med Genet
. 1995 Jan;
55(2):229-36.
PMID: 7717424
We present three probands with partial trisomies 2p21-23 due to ins(4;2)(q21;p21p23) pat, 2p23-pter due to t(2;4)(p23;q35)mat, and 2p21-pter due to t(2;11)(p21;q23.3)mat. More than 50 cases of partial trisomy 2p have...
4.
Lurie I, Rumyantseva N, Zaletajev D, Gurevich D, Korotkova I
J Genet Hum
. 1985 Jan;
33(1):67-75.
PMID: 3981145
Partial trisomy for the distal part of the short arm of chromosome 20 reported in a girl aged 11/2 years with typical craniofacial dysmorphies and psychomotor retardation. The trisomy resulted...