MARC

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001 SCIDIR_ocn899001536
003 OCoLC
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006 m o d
007 cr cn|||||||||
008 141124t19861986flua ob 101 0 eng d
040 |a E7B  |b eng  |e rda  |e pn  |c E7B  |d OCLCO  |d OCLCQ  |d UIU  |d OCLCF  |d YDXCP  |d EBLCP  |d N$T  |d OCLCO  |d OCL  |d OCLCO  |d OCLCQ  |d OCLCO  |d OCLCQ  |d STF  |d OCLCQ  |d OCLCO  |d COM  |d OCLCO  |d OCLCQ 
019 |a 895434182 
020 |a 9781483264486  |q (e-book) 
020 |a 1483264483  |q (e-book) 
020 |z 9780125628556 
035 |a (OCoLC)899001536  |z (OCoLC)895434182 
050 4 |a RG627  |b .P46 1986eb 
072 7 |a MED  |x 033000  |2 bisacsh 
082 0 4 |a 618.3/2042  |2 19 
111 2 |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. 
264 4 |c �1986 
300 |a 1 online resource (321 pages) :  |b illustrations. 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Birth Defects Institute Symposia 
504 |a Includes bibliographical references and index. 
588 0 |a Print version record. 
505 0 |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. 
505 8 |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. 
505 8 |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. 
505 8 |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. 
505 8 |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