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Yazar

Arsham, Marilyn S., editor.

(1)

Ashizawa, Tetsuo.

(1)

Barch, Margaret J., editor.

(1)

Berman, Jules J., author.

(1)

Bianchi, Filippo, 1964-

(1)

Brown, W. M. Court ort.yaz.

(1)

Carter, Ronald F.

(1)

De Rossi, Salvatore.

(1)

(1)

Konrad, Monica.

(1)

Lawce, Helen J., editor.

(1)

Le Beau, Michelle M. editor.

(1)

Luo, Zhengpeng, author.

(1)

Mann, Margaret W., author.

(1)

Matloff, Ellen T.

(1)

Milunsky, Aubrey, editor.

(1)

Milunsky, Jeff M., editor.

(1)

Mitelman, Felix.

(1)

Mittwoch, Ursula.

(1)

Ovid Technologies, Inc.

(1)

Parker, Michael.

(1)

Popkin, Daniel, author.

(1)

Rabbitts, Terence H. editor.

(1)

Rowley, Janet D. editor.

(1)

Schinzel, Albert, 1944-

(1)

Sharpe, Neil F.

(1)

(1)

SpringerLink (Online service)

(1)

(1)

Wells, R. D. (Robert D.)

(1)

Zneimer, Susan Mahler, author.

(1)

Tümünü genişlet

Dil

(18)

Yayın Yılı

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(1)

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Tümünü genişlet

Konu

Chromosome abnormalities.

(3)

Human chromosome abnormalities.

(3)

Handbooks and manuals.

(2)

Human chromosome abnormalities -- Diagnosis -- Moral and ethical aspects.

(2)

Human chromosome abnormalities -- Diagnosis -- Social aspects.

(2)

Human chromosome abnormalities -- Diagnosis.

(2)

Neoplasms -- genetics

(2)

Aberrations chromosomiques.

(1)

(1)

Biology -- Research.

(1)

Biomedical Research.

(1)

Biotechnology -- Law and legislation.

(1)

Cancer -- Genetic aspects.

(1)

Cancer Biology.

(1)

(1)

(1)

Chromosome Aberrations

(1)

Chromosome Aberrations.

(1)

Chromosome Disorders.

(1)

Chromosome abnormalities

(1)

Communication in public health.

(1)

Communication in science.

(1)

Cytogenetic Analysis -- methods

(1)

(1)

Cytogenetics -- Analysis.

(1)

Cytogenetics -- Laboratory manuals.

(1)

Cytogenetics -- methods

(1)

(1)

Cytogénétique -- Manuels de laboratoire.

(1)

(1)

DNA microarrays -- Analysis.

(1)

Data protection -- Law and legislation.

(1)

Deri Hastalıkları -- genetik -- El Kitapları

(1)

Dermatologic Agents -- therapeutic use

(1)

(1)

(1)

(1)

Diagnostics prénatals.

(1)

Fetus -- Abnormalities -- Genetic aspects

(1)

Fetus -- Abnormalities -- Genetic aspects.

(1)

Fetus -- Diseases -- Genetic aspects

(1)

Fetus -- Diseases -- Genetic aspects.

(1)

Fluorescence in situ hybridization.

(1)

Fœtus -- Maladies -- Aspect génétique.

(1)

Fœtus -- Malformations -- Aspect génétique.

(1)

Genetic Counseling

(1)

Genetic Diseases, Inborn.

(1)

Genetic Predisposition to Disease.

(1)

Genetic Testing

(1)

Genetic counseling.

(1)

Genetic engineering -- Law and legislation.

(1)

Genetic screening -- Social aspects.

(1)

(1)

(1)

Geschlechtsbestimmung

(1)

Guides et manuels.

(1)

(1)

Handbooks and manuals

(1)

Health literacy.

(1)

Human chromosome abnormalities -- Diagnosis -- Law and legislation.

(1)

Human genetics -- Government policy.

(1)

Human genetics -- Social aspects.

(1)

(1)

KROMOZOM ANOMALİLERİ.

(1)

(1)

LAW / Medical Law & Legislation.

(1)

Laboratory manuals

(1)

Laboratory manuals.

(1)

Medical genetics -- Law and legislation.

(1)

Medical genetics.

(1)

Medical records -- Access control.

(1)

Medicine -- Research.

(1)

Neoplasms -- prevention & control

(1)

Nervous System Diseases -- genetics.

(1)

Nervous system -- Diseases -- Genetic aspects.

(1)

(1)

Personalized medicine.

(1)

Pharmacogenetics.

(1)

Precision Medicine.

(1)

Prenatal Diagnosis

(1)

Prenatal diagnosis.

(1)

Privacy, Right of.

(1)

(1)

SCIENCE -- Life Sciences -- Biochemistry.

(1)

(1)

Self-examination, Medical.

(1)

Sex Determination (Analysis)

(1)

Sex chromosome abnormalities.

(1)

Sex chromosomes.

(1)

Sex differentiation, Genetic.

(1)

Skin Diseases -- diagnosis

(1)

Skin Diseases -- genetics -- Handbook

(1)

Skin Diseases -- therapy

(1)

Trinucleotide Repeats -- genetics.

(1)

(1)

(1)

manuals (instructional materials)

(1)

Tümünü genişlet

Materyal Türü

Shelf Location

Elektronik Kütüphane

Sağlık Bilimleri Genel Koleksiyon

Taylor Francis E-Kitap Koleksiyonu

Wiley E-Kitap Koleksiyonu

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13.

Aneuploidy etiology, disorders and risk factors için kapak resmi

Aneuploidy etiology, disorders and risk factors

Aneuploidy etiology, disorders and risk factors

Yazar

De Rossi, Salvatore. Bianchi, Filippo, 1964-

Yer Numarası

ONLINE

Elektronik Erişim

EBSCOhost http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=581818

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14.

Genetic testing care, consent, and liability için kapak resmi

Genetic testing care, consent, and liability

Genetic testing care, consent, and liability

Yazar

Sharpe, Neil F. Carter, Ronald F.

Yer Numarası

ONLINE

Elektronik Erişim

John Wiley http://dx.doi.org/10.1002/0471748897

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15.

Genetic instabilities and neurological diseases için kapak resmi

Genetic instabilities and neurological diseases

Genetic instabilities and neurological diseases

Yazar

Wells, R. D. (Robert D.) Ashizawa, Tetsuo.

Yer Numarası

ONLINE

Elektronik Erişim

ScienceDirect http://www.sciencedirect.com/science/book/9780123694621

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16.

Narrating the New Predictive Genetics Ethics, Ethnography and Science için kapak resmi

Narrating the New Predictive Genetics Ethics, Ethnography and Science

Narrating the New Predictive Genetics Ethics, Ethnography and Science

Yazar

Konrad, Monica.

Yer Numarası

ONLINE

Elektronik Erişim

Access by subscription

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17.

Genodermatoses : a clinical guide to genetic skin disorders için kapak resmi

Genodermatoses : a clinical guide to genetic skin disorders

Genodermatoses : a clinical guide to genetic skin disorders

Yazar

Spitz, Joel L.

Yer Numarası

WR 39 G335 2005

Format:

Durum

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18.

Catalogue of unbalanced chromosome aberrations in man için kapak resmi

Catalogue of unbalanced chromosome aberrations in man

Catalogue of unbalanced chromosome aberrations in man

Yazar

Schinzel, Albert, 1944-

Yer Numarası

QS 677 S336 2001

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19.

Genetics of sex differentiation için kapak resmi

Genetics of sex differentiation

Genetics of sex differentiation

Yazar

Mittwoch, Ursula.

Yer Numarası

ONLINE

Elektronik Erişim

ScienceDirect http://www.sciencedirect.com/science/book/9780125010405

Format:

Durum

Çevrimiçi Kütüphane~1

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