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Results of search for 'su:"Monosomy"', page 3 of 84
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Authors
Ballif, Blake C
Berger, R
Cantú, J M
Chen, C P
Chen, Chih-Ping
Chern, Schu-Rern
Dewald, G W
Dutrillaux, B
Espinet, Blanca
Fenaux, P
Florensa, Lourdes
Fonatsch, C
Fryns, J P
Germing, Ulrich
Imaizumi, K
Ohashi, H
Rivera, H
Shaffer, Lisa G
Solé, Francesc
Wang, Wayseen
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Adolescent
Adult
Aged
Child
Child, Preschool
Chromosome Aberrations
Chromosome Deletion
Chromosomes, Human, Pair 7
Female
Humans
In Situ Hybridization, Fluorescence
Karyotyping
Male
Middle Aged
Monosomy
Myelodysplastic Syndromes
Translocation, Genetic
Trisomy
diagnosis
genetics
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41.
Should embryos with autosomal monosomy by preimplantation genetic testing for aneuploidy be transferred?: Implications for embryo selection from a systematic literature review of autosomal monosomy survivors.
[electronic resource]
by
Bunnell, M E
Wilkins-Haug, L
Reiss, R
Producer:
20181022
In:
Prenatal diagnosis
vol. 37
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42.
[Resolving capacity of monosomic line analysis in cytogenetic studies of common wheat].
[electronic resource]
by
Zharkov, N A
Producer:
20050314
In:
TSitologiia i genetika
vol. 38
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43.
Activation of rye 5RL neocentromere by an organophosphate pesticide.
[electronic resource]
by
Cuacos, M
González-García, M
González-Sánchez, M
Puertas, M J
Vega, J M
Producer:
20110708
In:
Cytogenetic and genome research
vol. 134
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44.
Fatal Outcome in a Newborn Calf Associated with Partial Trisomy 25q and Partial Monosomy 11q, 60,XX,der(11)t(11;25)(q11;q14∼21).
[electronic resource]
by
Iannuzzi, Alessandra
Genualdo, Viviana
Perucatti, Angela
Pauciullo, Alfredo
Varricchio, Giovanna
Incarnato, Domenico
Matassino, Donato
Iannuzzi, Leopoldo
Producer:
20160122
In:
Cytogenetic and genome research
vol. 146
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45.
Chromosome 22 mosaic monosomy (46,XY/45,XY,-22).
[electronic resource]
by
Verloes, A
Herens, C
Lambotte, C
Frederic, J
Producer:
19871207
In:
Annales de genetique
vol. 30
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46.
Granulocyte function in myelodysplastic syndromes.
[electronic resource]
by
Ruutu, P
Producer:
19860520
In:
Scandinavian journal of haematology. Supplementum
vol. 45
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47.
False negative fetal cell free DNA screening for microdeletion syndromes in the presence of an unbalanced translocation involving monosomy 4p.
[electronic resource]
by
Qi, Zhongxia
Madaan, Shreshtha
Chetty, Shilpa
Yu, Jingwei
Wiita, Arun P
Producer:
20180426
In:
Prenatal diagnosis
vol. 37
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48.
Infertility associated with monosomy-X in a crossbred cattle heifer.
[electronic resource]
by
Prakash, B
Balain, D S
Lathwal, S S
Malik, R K
Producer:
19960228
In:
The Veterinary record
vol. 137
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49.
Craniosynostosis in the Ullrich-Turner syndrome.
[electronic resource]
by
Heinrichs, C
Elmer, C
Derasse, M
Perlmutter, N
Vamos, E
Producer:
19911024
In:
American journal of medical genetics
vol. 40
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50.
[Partial deletion 10qter. A new case].
[electronic resource]
by
Vanlieferinghen, P
Dechelotte, P
Charbonné, F
Producer:
19871214
In:
Annales de genetique
vol. 30
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51.
Turner syndrome and haploinsufficiency.
[electronic resource]
by
Zinn, A R
Ross, J L
Producer:
19981106
In:
Current opinion in genetics & development
vol. 8
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52.
Growth hormone supplementation in Turner's syndrome.
[electronic resource]
by
Van Vliet, G
Deal, C
Producer:
19990113
In:
The Journal of pediatrics
vol. 133
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53.
Single-cell dissection of monosomy 7 syndromes.
[electronic resource]
by
Gutierrez-Perez, Irene
Bryceson, Yenan T
Producer:
20180118
In:
Blood
vol. 130
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54.
Monosomy E3 in a feline basal cell tumour.
[electronic resource]
by
Ortner, B M
Reifinger, G L
Producer:
19960318
In:
The Journal of small animal practice
vol. 36
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55.
[AUTOSOMAL MONOSOMY OF THE 6-12 GROUP SIMULATING MULTIPLE ABNORMALITIES].
[electronic resource]
by
MIELER, W
Producer:
19961201
In:
Folia haematologica (Leipzig, Germany : 1928)
vol. 82
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56.
On the parental origin of de novo mutation in man.
[electronic resource]
by
Chandley, A C
Producer:
19910828
In:
Journal of medical genetics
vol. 28
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57.
Genetic factors of recurrent abortions.
[electronic resource]
by
Cammarata, M
Corsello, G
Marino, M
Morabito, M
Pecoraro, M R
Piccione, M
Giuffrè, L
Producer:
19910523
In:
Acta Europaea fertilitatis
vol. 20
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58.
[Bilateral gonadoblastoma in a case of Turner syndrome with 40,XO monosomy].
[electronic resource]
by
Schütz, M
Köhler, G
Lorenz, G
Producer:
19841109
In:
Zentralblatt fur Gynakologie
vol. 106
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59.
Allelotype of human bladder cancer.
[electronic resource]
by
Knowles, M A
Elder, P A
Williamson, M
Cairns, J P
Shaw, M E
Law, M G
Producer:
19940209
In:
Cancer research
vol. 54
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60.
Ullrich-Turner syndrome: seven pregnancies in an apparent 45,X woman.
[electronic resource]
by
Magee, A C
Nevin, N C
Armstrong, M J
McGibbon, D
Nevin, J
Producer:
19980227
In:
American journal of medical genetics
vol. 75
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