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180813s1971 mau|||| |||| 00| 0|eng |
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|a 9780031652225
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|a 0031652225
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|a donación
|f papel
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|a Sistema de Bibliotecas de la Universidad de Panamá
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0 |
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|a QH 605
|b L578 1971
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082 |
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|q SIBIUP
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100 |
1 |
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|a Levine, Harry
|9 197140
|e autor
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245 |
1 |
0 |
|a Clinical cytogenetics
|c / Harry Levine.
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250 |
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|a Primera edición
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264 |
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4 |
|a Boston :
|b Little, Brown and Company,
|c ©1971
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300 |
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|a x, 572 páginas :
|b ilustraciones ;
|c 25 cm
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336 |
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|2 rdacontent
|a texto
|b txt
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337 |
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|2 rdamedia
|a sin mediación
|b n
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338 |
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|2 rdacarrier
|a volumen
|b nc
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504 |
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|a Incluye bibliografía e índice
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505 |
2 |
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|a Human chromosomes and Their Identification. -- Normal Cell Division. -- Abnormal Cell Division. -- Sex Chromatin (Barr Body). --Nature of the Sex Chromatin.-- Polymorphonuclear Neutrophil “Drumstick”. -- Introduction to Human Chromosomal Aberrations. -- Sex Chromosomal Abnormalities. -- Karyotype-Phenotype Correlations in Gonadal Dysgenesis: Implications in the Pathogénesis of Malformations and of Other Types of Abnormal Gonadal Development. -- Autosomal Abnormalities. -- Group A (1-3) Chomosomal Anomalies. -- Group B (4-5) Chomosomal Anomalies. -- Group C (6-12) Chomosomal Anomalies. -- Group D (13-15) Chomosomal Anomalies. -- Group E (16-18) Chomosomal Anomalies. -- Group F (19-20) Chomosomal Anomalies. -- Group G (21-22) Chomosomal Anomalies. -- Polyploidy. -- Human Disorders Occasionally Associated with a Detectable Chromosomal Aberration. -- Inherited Disorders Associated with a High Frequency of Chromosome Breakage and an Increased Risk of Malignancy, Particularly Leukemia. -- Genetic Counseling in Relation to Chromosomal Abnormalities. -- Dermatoglyphics
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650 |
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|a CITOGENETICA
|2 DCS
|9 197843
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650 |
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|9 160220
|a ABERRACION CROMOSOMICA
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|e donación
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|r 2017-01-17
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|w 2017-01-17
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