L Hudgins
Overview
Explore the profile of L Hudgins including associated specialties, affiliations and a list of published articles.
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27
Citations
464
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Recent Articles
1.
Allyse M, Sayres L, Havard M, King J, Greely H, Hudgins L, et al.
Prenat Diagn
. 2013 Apr;
33(7):656-61.
PMID: 23613322
Objective: The goal of this study is to provide an ethical framework for clinicians and companies providing noninvasive prenatal testing using cell-free fetal DNA or whole fetal cells. Method: In...
2.
Blumenfeld Y, Taylor J, Lee H, Hudgins L, Sung J, El-Sayed Y
J Perinatol
. 2012 Mar;
32(12):907-12.
PMID: 22402484
Objective: In 2009, the California Genetic Disease Branch introduced an aneuploidy screening program allowing Medi-Cal (state insured) patients access to state-sponsored first-trimester screening. The objective of this study was to...
3.
Battaglia A, Chen Z, Brothman A, Morelli S, Palumbos J, Carey J, et al.
Am J Med Genet A
. 2005 Mar;
134(3):334-7.
PMID: 15759263
No abstract available.
4.
Adam M, Hudgins L
Clin Genet
. 2005 Feb;
67(3):209-19.
PMID: 15691356
Kabuki syndrome (KS) (Kabuki make-up syndrome, Niikawa-Kuroki syndrome) is a multiple malformation/mental retardation syndrome that was described initially in Japan but is now known to occur in many other ethnic...
5.
Rosenberg M, Killoran C, Dziadzio L, Chang S, Stone D, Meck J, et al.
Hum Genet
. 2001 Nov;
109(3):311-8.
PMID: 11702212
We screened 120 children with sporadic multiple congenital anomalies and either growth or mental retardation for uniparental disomy (UPD) or subtelomeric deletions. The screening used short tandem repeat polymorphisms (STRP)...
6.
Hahn J, Henry M, Hudgins L, Madan A
Pediatrics
. 2001 Nov;
108(5):E95.
PMID: 11694679
We report a case of congenital hypomyelination neuropathy presenting at birth. The infant had generalized hypotonia and weakness. There was decreased respiratory effort along with a right phrenic nerve and...
7.
Parisi M, Dinulos M, Leppig K, Sybert V, Eng C, Hudgins L
J Med Genet
. 2001 May;
38(1):52-8.
PMID: 11332402
No abstract available.
8.
Hudgins L, Geer J, Cassidy S
Genet Med
. 2001 Mar;
1(1):49-51.
PMID: 11261430
We report on 10 African Americans with Prader-Willi syndrome whose features differ from those of white patients with this condition. Growth is less affected, hand and foot lengths usually are...
9.
Bennett R, Hudgins L, SMITH C, Motulsky A
Genet Med
. 2001 Mar;
1(6):286-92.
PMID: 11258630
Purpose: To determine current practices of genetic counseling and screening for consanguineous couples, their pregnancies and children, and to compare these practices to recommendations in the literature. Methods: A questionnaire...
10.
Erlich M, Cunningham M, Hudgins L
Am J Med Genet
. 2000 Dec;
95(3):269-74.
PMID: 11102934
We report the first observation of parent-to-child transmission of dysgnathia, a rare disorder characterized by severe mandibular hypoplasia or agenesis, ear anomalies, microstomia, and microglossia. Patient 1 was noted prenatally...