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141124t19861986flua ob 101 0 eng d |
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|a 895434182
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|a 9781483264486
|q (e-book)
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|a 1483264483
|q (e-book)
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|z 9780125628556
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|a (OCoLC)899001536
|z (OCoLC)895434182
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|a RG627
|b .P46 1986eb
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|a MED
|x 033000
|2 bisacsh
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|a 618.3/2042
|2 19
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|a New York State Health Department Birth Defects Symposium
|n (15th :
|d 1984 :
|c Albany, N.Y.)
|
245 |
1 |
0 |
|a Perinatal genetics :
|b diagnosis and treatment /
|c edited by Ian H. Porter, Norma H. Hatcher, Ann M. Willey.
|
264 |
|
1 |
|a Orlando, Florida ;
|a London, England :
|b Academic Press, Inc.,
|c 1986.
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264 |
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4 |
|c �1986
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300 |
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|a 1 online resource (321 pages) :
|b illustrations.
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336 |
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|a text
|b txt
|2 rdacontent
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337 |
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|a computer
|b c
|2 rdamedia
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338 |
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|a online resource
|b cr
|2 rdacarrier
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490 |
1 |
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|a Birth Defects Institute Symposia
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504 |
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|a Includes bibliographical references and index.
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588 |
0 |
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|a Print version record.
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505 |
0 |
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|a Front Cover; Perinatal Genetics: Diagnosis and Treatment; Copyright Page; Table of Contents; Preface; Acknowledgements; SECTION I: PREGNANCY LOSS; CHAPTER 1. VERY EARLY PREGNANCY: FERTILIZATION AND IMPLANTATION FREQUENCY AND CAUSE OF LOSS; INTRODUCTION; THE PROBABILITY OF FERTILIZATION; THE FREQUENCY OF REPRODUCTIVE LOSS; EXPECTATIONS OF SURVIVAL AND LOSS AT EACH STAGE OF GESTATION; THE CONTRIBUTION OF ANEUPLOID* ANOMALIES TO EARLY LOSS; CONCLUSION; REFERENCES; CHAPTER 2. CYTOGENETIC ABNORMALITIES IN SPONTANEOUS ABORTIONS OF RECOGNIZED CONCEPTIONS; REFERENCES.
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505 |
8 |
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|a CHAPTER 3. REPETITIVE SPONTANEOUS ABORTIONI. RECURRENCE RISKS; III. CAUSES OF REPETITIVE ABORTIONS; IV. RECOMMENDED CLINICAL EVALUATION; REFERENCES; SECTION II: PRENATAL DIAGNOSIS (Including Chorion Villus Sampling); CHAPTER 4. PRENATAL DIAGNOSIS OF THE FRAGILE X SYNDROME; PRENATAL DIAGNOSIS OF THE FRAGILE X SYNDROME; METHODS; RESULTS; FAMILY HISTORY OF FRA (X) SYNDROME; REFERENCES; CHAPTER 5. PRENATAL DIAGNOSIS AND CARRIER DETECTION OF CLASSICAL PHENYLKETONURIA; SUMMARY; ACKNOWLEDGEMENT; REFERENCES; CHAPTER 6. PRENATAL GENETIC DIAGNOSIS BYCHORIONIC VILLUS SAMPLING; INTRODUCTION.
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505 |
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|a I. History of Chorionic Villus Sampling (CVS)II. Sampling Procedure; III. Cytogenetic Methods; IV. Biochemical Methods; V. Results; VI. Discussion; REFERENCES; SECTION III: PRENATAL MANAGEMENT AND TREATMENT; CHAPTER 7. PRENATAL TREATMENT OF BIOCHEMICAL DISORDERS; Antenatal Therapy for Metabolic Disorders; Methylmalonic Acidemia (MMA); Multiple Carboxylase Deficiency; Abnormalities of Mineral Metabolism; Galactosemia; Congential Adrenal Hyperplasia (CAH); Miscellany and Speculation; REFERENCES; CHAPTER 8. FETAL SURGERY, OLD CONTROVERSIES ABOUT NEW THERAPIES; INTRODUCTION; FETAL TRANSFUSIONS.
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505 |
8 |
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|a Current problemswhere do we go from here; references; chapter 9. diagnosis and management of ambiguous genitalia in the newborn; normal sexual development; female pseudohermaphroditism; male pseudohermaphroditism; disorders of testosterone biosynthesis; disorders of testosterone metabolism; other unclassified forms of male pseudohermaphroditism; management of the patient with ambiguous genitalia; references; chapter 10. current perspectives onfetal hydrocephalus; diagnosis; outcome; management; references; section iv: in vitro fertilization and sex determination.
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505 |
8 |
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|a Chapter 11. in vitro fertilization and embryo transferrecruitment and selection of the dominant follicle; stimulation of the ovarian/menstrual cycle; references; chapter 12. h-y antigen, sex determination and gender control; a. introduction; b. h-y and the testis; c. abnormalities of sex determination; d. new techniques in the study of sex determination; e. h-y in the control of sex ratio; references; section v: miscellaneous; chapter 13. environmental factors and human birth defects: interpretation of relative risks in clinical genetics; addendum-january 1986; acknowledgements; references.
|
650 |
|
0 |
|a Fetus
|x Abnormalities
|x Genetic aspects
|v Congresses.
|
650 |
|
0 |
|a Prenatal diagnosis
|v Congresses.
|
650 |
|
0 |
|a Fetus
|x Abnormalities
|x Treatment
|v Congresses.
|
650 |
|
0 |
|a Genetic counseling
|v Congresses.
|
650 |
|
0 |
|a Abortion
|x Moral and ethical aspects
|v Congresses.
|
650 |
|
6 |
|a F�tus
|0 (CaQQLa)201-0110517
|x Malformations
|0 (CaQQLa)201-0110517
|x Aspect g�en�etique
|0 (CaQQLa)201-0377534
|v Congr�es.
|0 (CaQQLa)201-0378219
|
650 |
|
6 |
|a Diagnostics pr�enatals
|0 (CaQQLa)201-0039133
|v Congr�es.
|0 (CaQQLa)201-0378219
|
650 |
|
6 |
|a F�tus
|0 (CaQQLa)201-0110517
|x Malformations
|0 (CaQQLa)201-0110517
|x Traitement
|0 (CaQQLa)201-0377521
|v Congr�es.
|0 (CaQQLa)201-0378219
|
650 |
|
6 |
|a Conseil g�en�etique
|0 (CaQQLa)201-0039132
|v Congr�es.
|0 (CaQQLa)201-0378219
|
650 |
|
6 |
|a Avortement
|0 (CaQQLa)201-0033208
|x Aspect moral
|0 (CaQQLa)201-0033208
|v Congr�es.
|0 (CaQQLa)201-0378219
|
650 |
|
7 |
|a MEDICAL
|x Gynecology & Obstetrics.
|2 bisacsh
|
650 |
|
7 |
|a Abortion
|x Moral and ethical aspects.
|2 fast
|0 (OCoLC)fst00794606
|
650 |
|
7 |
|a Fetus
|x Abnormalities
|x Genetic aspects.
|2 fast
|0 (OCoLC)fst00923432
|
650 |
|
7 |
|a Fetus
|x Abnormalities
|x Treatment.
|2 fast
|0 (OCoLC)fst00923435
|
650 |
|
7 |
|a Genetic counseling.
|2 fast
|0 (OCoLC)fst00940001
|
650 |
|
7 |
|a Prenatal diagnosis.
|2 fast
|0 (OCoLC)fst01075465
|
655 |
|
2 |
|a Congress
|0 (DNLM)D016423
|
655 |
|
7 |
|a Conference papers and proceedings.
|2 fast
|0 (OCoLC)fst01423772
|
655 |
|
7 |
|a Conference papers and proceedings.
|2 lcgft
|
655 |
|
7 |
|a Actes de congr�es.
|2 rvmgf
|0 (CaQQLa)RVMGF-000001049
|
700 |
1 |
|
|a Porter, Ian H.,
|e editor.
|
700 |
1 |
|
|a Hatcher, Norma H.,
|e editor.
|
700 |
1 |
|
|a Willey, Ann M.,
|e editor.
|
776 |
0 |
8 |
|i Print version:
|a New York State Health Department. Birth Defects Symposium (15th : 1984 : Albany, N.Y.).
|t Perinatal genetics : diagnosis and treatment.
|d Orlando, Florida ; London, England : Academic Press, Inc., �1986
|h xi, 308 pages
|k Birth Defects Institute symposia.
|z 9780125628556
|
830 |
|
0 |
|a Birth Defects Institute symposia.
|
856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780125628556
|z Texto completo
|