Results 161 to 170 of about 1,112,704 (347)
Juvenile Form of Adrenogenital Syndrome [PDF]
, 1939 J. Steven Richardson, W Döll
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The Young and the Redemptionless? Juvenile Offenders Before Miller v. Alabama [PDF]
, 2016 The Eighth Amendment to the U.S. Constitution prohibits excessive criminal sanctions, and the Supreme Court has held that this provision has special application in situations dealing with juvenile offenders.
Johnson, Katherine
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Gastrointestinal defects and immunodeficiency syndrome 1 (GIDID1) is a rare autosomal recessive disorder caused by biallelic variants in TTC7A. GIDID1 is characterized by a broad clinical spectrum ranging from very early‐onset inflammatory bowel disease (VEOIBD) to multiple intestinal atresia (MIA) with or without immunological manifestations.
Julia Imhoff +8 more
wiley +1 more source
Intestinal Atresia in PPP1R12A‐Related Urogenital and Brain Malformation Syndrome
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT PPP1R12A‐related urogenital and brain malformation syndrome (UBMS) is a newly described disorder characterized by congenital anomalies primarily involving the urogenital system and the brain. We describe a preterm female neonate with multiple congenital anomalies, including type IIIb jejunal atresia, incomplete intestinal rotation, imperforate
Adriana Gomes +4 more
wiley +1 more source
JJDP Monitoring Data — 1988: JJDP Violations and Juvenile Detention Counts for Lockups, Jails, Adult Correctional Facilities and Juvenile Detention Centers [PDF]
, 1990 This data supplement to the 1988 Juvenile Justice and Delinquency Prevention Act Compliance Monitoring Report (Mar 1990) presents data on 1988 violations in Alaska of the Juvenile Justice and Delinquency Prevention Act (JJDPA), which mandates removal of
Parry, David L.
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim +9 more
wiley +1 more source
Juvenile Skipjack from the Stomach Contents of Tunas and Marlins
, 1953 Akira Suda
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Potential use of offshore marine structures in rebuilding an overfished rockfish species, bocaccio (Sebastes paucispinis) [PDF]
, 2006 Although bocaccio (Sebastes paucispinis) was an economically important rockfish species along the west coast of North America, overfishing has reduced the stock to about 7.4% of its former unfished population. In 2003, using a manned research submersible,
Bull, Ann Scarborough +5 more
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