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Obstetric Anesthesia Digest, ISSN 0275-665X, 12/2017, Volume 37, Issue 4, p. 177
(BJOG 2017;124:584-594)Testing for acidosis at all deliveries is advocated by some as an early and effective way to identify infants at risk for a range of... 
Journal Article
The Journal of Maternal-Fetal & Neonatal Medicine, ISSN 1476-7058, 05/2018, Volume 31, Issue 10, pp. 1272 - 1278
Purpose: To investigate the utility of umbilical artery (UA) lactate measurements in a South African hospital for assessing intrapartum care and predicting... 
neonatal | resuscitation | South Africa | intrapartum | Lactate | VENOUS LACTATE | TERM | PREDICTION | OBSTETRICS & GYNECOLOGY | ENCEPHALOPATHY | ARTERIAL | 5-MINUTE APGAR SCORE | BLOOD LACTATE | 2ND-STAGE | FETAL
Journal Article
BJOG: An International Journal of Obstetrics & Gynaecology, ISSN 1470-0328, 01/2018, Volume 125, Issue 2, pp. 212 - 224
Journal Article
10/2008, Monographs in Human Genetics, ISBN 9783805586535, Volume 17, 11
Noonan syndrome is an autosomal dominant condition notable both for its common occurrence and phenotypic variability. It is characterized by short stature,... 
Chapter
Book Chapter
Journal of Medical Genetics, ISSN 0022-2593, 1987, Volume 24, Issue 1, pp. 9 - 13
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 11/1998, Volume 35, Issue 11, pp. 920 - 923
Both Miller-Dieker syndrome and isolated lissencephaly sequence are associated with classical lissencephaly. Both have been shown to be associated with... 
Lissencephaly | Pattern profiles | Miller-Dieker syndrome | lissencephaly | MALFORMATIONS | GENE | pattern profiles | GENETICS & HEREDITY | LIS1 | CHROMOSOME-17P13 | DELETION
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 1998, Volume 179, Issue 1, pp. 277 - 278
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 11/1991, Volume 28, Issue 11, pp. 752 - 756
Journal Article
Clinical Genetics, ISSN 0009-9163, 05/1986, Volume 29, Issue 5, pp. 429 - 433
Two sisters with Apert acrocephalosyndactyly syndrome born to normal unrelated parents are described. Paternity studies show that the probability of paternity... 
germinal mosaicism | mutation | Acrocephalosyndactyly | Apert syndrome | Humans | Child, Preschool | Female | Infant | Mosaicism | Acrocephalosyndactylia - genetics | Germ Cells - ultrastructure | Mutation
Journal Article
Clinical Genetics, ISSN 0009-9163, 09/1986, Volume 30, Issue 3, pp. 150 - 153
Growth retardation is a relatively consistent feature of Noonan syndrome but a standardized growth curve for height has never been calculated. Analysis of... 
growth patterns | Growth | male Turner Syndrome | Noonan syndrome | height | Noonan Syndrome - pathology | Humans | Adolescent | Child, Preschool | Body Height | Female | Infant | Male | Reference Values | Child | Infant, Newborn
Journal Article