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Results of search for 'au:"WAJNTAL, A"', page 1 of 2
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Authors
Alves, R S
Bagnolli, V R
Billerbeck, A E
Bisi, H
Burke, T
Capelozzi, V L
Diament, A
Diament, A J
Gonzalez, C H
Kim, C A
Koiffmann, C P
Miyaki, C Y
Moretti-Ferreira, D
Saldanha, P H
Souza, D H
Toledo, S P
Vianna-Morgante, A M
Wajntal, A
de Campos, E P
de Souza, D H
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Banding
Chromosome Disorders
Dermatoglyphics
Female
Humans
Infant
Intellectual Disability
Karyotyping
Male
Phenotype
Syndrome
Translocation, Genetic
abnormalities
genetics
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English
Portuguese
Your search returned 32 results.
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1.
[True hermaphroditism: comments on its etiology (author's transl)].
[electronic resource]
by
Wajntal, A
Producer:
19770428
In:
Revista brasileira de pesquisas medicas e biologicas
vol. 10
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2.
A tetrazolium method for distinguishing between cultured human fibroblasts having eiter normal or deficient levels of glucose-6-phosphate dehydrogenase.
[electronic resource]
by
Wajntal, A
DeMars, R
Producer:
19690508
In:
Biochemical genetics
vol. 1
Online resources:
Available from publisher's website
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3.
47XX, + 13/46,XX mosaicism: a case report.
[electronic resource]
by
Toledo, S P
Wajntal, A
Producer:
19771125
In:
Acta geneticae medicae et gemellologiae
vol. 26
Online resources:
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4.
Mutation rates of the abnormal hemoglobin genes.
[electronic resource]
by
FROTA-PESSOA, O
WAJNTAL, A
Producer:
19981101
In:
American journal of human genetics
vol. 15
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5.
[Frequency of aneuploid zygotes in human fertilization].
[electronic resource]
by
Wajntal, A
Saldanha, P H
Producer:
19780929
In:
Revista paulista de medicina
vol. 91
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6.
Chromosome aberrations in Sotos syndrome.
[electronic resource]
by
Wajntal, A
Koiffmann, C P
Producer:
19920312
In:
Clinical genetics
vol. 40
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7.
Median cleft face syndrome or frontonasal dysplasia: a case report with associated kidney malformation.
[electronic resource]
by
Roizenblatt, J
Wajntal, A
Diament, A J
Producer:
19790716
In:
Journal of pediatric ophthalmology and strabismus
vol. 16
Online resources:
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8.
Pathologic findings in the Wolf-Hirschhorn (4p-) syndrome.
[electronic resource]
by
Gonzalez, C H
Capelozzi, V L
Wajntal, A
Producer:
19811122
In:
American journal of medical genetics
vol. 9
Online resources:
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9.
[Pyle's syndrome with chromosome breakage].
[electronic resource]
by
Diament, A J
Wajntal, A
Saldanha, P H
Producer:
19720425
In:
Arquivos de neuro-psiquiatria
vol. 29
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10.
A ring D chromosome in association with Down's syndrome-like phenotype.
[electronic resource]
by
Wajntal, A
Diament, A J
Saldanha, P H
Producer:
19730806
In:
Arquivos de neuro-psiquiatria
vol. 31
Online resources:
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11.
DNA fingerprinting in the rare black-fronted piping guan Pipile jacutinga (Cracidae, Aves).
[electronic resource]
by
Pereira, S L
Miyaki, C Y
Wajntal, A
Producer:
19971030
In:
Revista brasileira de biologia
vol. 56
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12.
Comparison of weight responses to testosterone propionate in patients with male pseudohermaphroditism and controls of different age groups.
[electronic resource]
by
Epps, D R
Wajntal, A
de Campos, E P
Producer:
19750822
In:
Revista do Hospital das Clinicas
vol. 30
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13.
Interstitial cell tumor and gynecomastia in familial male pseudohermaphroditism due to a defect in androgen biosynthesis.
[electronic resource]
by
Epps, D
de Campos, E P
Wajntal, A
Lodovici, O
Producer:
19780828
In:
Revista do Hospital das Clinicas
vol. 33
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14.
Sex typing of Aratinga parrots using the human minisatellite probe 33.15.
[electronic resource]
by
Miyaki, C Y
Hanotte, O
Wajntal, A
Burke, T
Producer:
19921125
In:
Nucleic acids research
vol. 20
Online resources:
Available from publisher's website
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15.
[Role of chromosome changes in the etiology of male infertility].
[electronic resource]
by
Soares-Vieira, J A
Wajntal, A
Koiffmann, C P
Producer:
19890727
In:
Revista paulista de medicina
vol. 106
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16.
Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
[electronic resource]
by
Koiffmann, C P
Wajntal, A
Huyke, B J
Castro, R M
Producer:
19880505
In:
American journal of medical genetics
vol. 29
Online resources:
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17.
Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).
[electronic resource]
by
Gonzalez, C H
Billerbeck, A E
Takayama, L C
Wajntal, A
Producer:
19830407
In:
American journal of medical genetics
vol. 14
Online resources:
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18.
A 15/17 translocation in a patient with Prader-Labhart-Willi syndrome.
[electronic resource]
by
Cavalli, I J
Sbalqueiro, I J
Wajntal, A
Freire-Maia, N
Producer:
19821021
In:
Human heredity
vol. 32
Online resources:
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19.
Macrosomia, obesity, macrocephaly and ocular abnormalities (MOMO syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndrome.
[electronic resource]
by
Moretti-Ferreira, D
Koiffmann, C P
Listik, M
Setian, N
Wajntal, A
Producer:
19930730
In:
American journal of medical genetics
vol. 46
Online resources:
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20.
Ring chromosome 7 in a man with multiple congenital anomalies and mental retardation.
[electronic resource]
by
Koiffmann, C P
Diament, A
de Souza, D H
Wajntal, A
Producer:
19901010
In:
Journal of medical genetics
vol. 27
Online resources:
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