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Refinado por: data de publicação: 1976Até1992 remover xxx: xxx remover Japonês remover Inglês remover
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1
47,XXX: what is the prognosis?
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Artigo
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47,XXX: what is the prognosis?

Linden, M G ; Bender, B G ; Harmon, R J ; Mrazek, D A ; Robinson, A

Pediatrics (Evanston), 1988-10, Vol.82 (4), p.619-630 [Periódico revisado por pares]

United States

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2
CHEMOTHERAPY IN BILIARY TRACT INFECTIONS (XXX): SPECIAL REFERENCE TO THE CONCENTRATION OF MICRONOMICIN IN HUMAN GALLBLADDER TISSUES AND BILE
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CHEMOTHERAPY IN BILIARY TRACT INFECTIONS (XXX): SPECIAL REFERENCE TO THE CONCENTRATION OF MICRONOMICIN IN HUMAN GALLBLADDER TISSUES AND BILE

YOTSUMOTO, FUMIAKI ; KATO, HIROAKI ; TANIMURA, HIROSHI ; NAKANO, MASAHIKO ; YUNG, MITSUTOSHI ; SETOYAMA, MOTOICHI ; MUKAIHARA, SUMIO

The Japanese Journal of Antibiotics, 1985/11/25, Vol.38(11), pp.3087-3096 [Periódico revisado por pares]

Japan: Japan Antibiotics Research Association

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3
An extra maternally derived X chromosome is deleterious to early mouse development
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An extra maternally derived X chromosome is deleterious to early mouse development

Shao, C ; Takagi, N

Development (Cambridge), 1990-11, Vol.110 (3), p.969-975 [Periódico revisado por pares]

England: The Company of Biologists Limited

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4
Identification of differing etiologies of clinically diagnosed premature menopause
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Identification of differing etiologies of clinically diagnosed premature menopause

Board, John A. ; Redwine, Fay O. ; Moncure, Charles W. ; Frable, William J. ; Taylor, John R.

American journal of obstetrics and gynecology, 1979-08, Vol.134 (8), p.936-944 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Unusually long survival in a case of full triploidy of maternal origin
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Artigo
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Unusually long survival in a case of full triploidy of maternal origin

Fryns, J P ; van de Kerckhove, A ; Goddeeris, P ; van den Berghe, H

Human genetics, 1977-01, Vol.38 (2), p.147-155 [Periódico revisado por pares]

Germany

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6
Four new cases of ring 21 and 22 including familial transmission of ring 21
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Artigo
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Four new cases of ring 21 and 22 including familial transmission of ring 21

Palmer, C G ; Hodes, M E ; Reed, T ; Kojetin, J

Journal of medical genetics, 1977-02, Vol.14 (1), p.54-60 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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7
Isodicentric (X)(q13): A new characteristic chromosomal anomaly in myeloproliferative syndrome?
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Isodicentric (X)(q13): A new characteristic chromosomal anomaly in myeloproliferative syndrome?

Petit, P. ; Fryns, J.P. ; Masure, R. ; Van Den Berghe, H.

Cancer genetics and cytogenetics, 1982-12, Vol.7 (4), p.339-341

United States: Elsevier Inc

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8
Interference in the Stroop color-naming task
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Artigo
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Interference in the Stroop color-naming task

Yamazaki, A

Shinrigaku kenkyū, 1985-10, Vol.56 (4), p.185-191 [Periódico revisado por pares]

Japan

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9
Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors
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Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors

Kallioniemi, Anne ; Olli-P. Kallioniemi ; Sudar, Damir ; Rutovitz, Denis ; Gray, Joe W. ; Waldman, Fred ; Pinkel, Dan

Science (American Association for the Advancement of Science), 1992-10, Vol.258 (5083), p.818-821 [Periódico revisado por pares]

WASHINGTON: American Society for the Advancement of Science

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10
A Conserved Double-Stranded RNA-Binding Domain
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A Conserved Double-Stranded RNA-Binding Domain

St Johnston, Daniel ; Brown, Nicholas H. ; Gall, Joseph G. ; Jantsch, Michael

Proceedings of the National Academy of Sciences - PNAS, 1992-11, Vol.89 (22), p.10979-10983 [Periódico revisado por pares]

WASHINGTON: National Academy of Sciences of the United States of America

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