Works matching IS 15524841 AND DT 2024 AND VI 195 AND IP 6

Results: 8

The effectiveness of psychiatric genetic counseling training: An analysis of 13 international workshops.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 6, p. 1, doi. 10.1002/ajmg.b.32978
By:
- Mack, Tiera;
- Batallones, Rolan;
- Morris, Emily;
- Inglis, Angela;
- Moldovan, Ramona;
- McGhee, Kevin;
- Zimmerman, Kip D.;
- Austin, Jehannine
Publication type:
Article
Luxenburger's 1939 Essay on "Schizophrenia and its Hereditary Circle".
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 6, p. 1, doi. 10.1002/ajmg.b.32977
By:
- Kendler, Kenneth S.;
- Klee, Astrid
Publication type:
Article
Issue Information ‐ TOC.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 6, p. 1, doi. 10.1002/ajmg.b.32945
Publication type:
Article
Mental health, coping, and protective factors in mothers of children with 22q11.2 deletion syndrome.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 6, p. 1, doi. 10.1002/ajmg.b.32973
By:
- McBride, Haley;
- Jhawar, Nandini;
- Boucicaut, Laurie;
- Bearden, Carrie E.;
- Kates, Wendy R.;
- Woolf‐King, Sarah E.;
- Antshel, Kevin M.
Publication type:
Article
Retraction: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 6, p. 1, doi. 10.1002/ajmg.b.32972
Publication type:
Article
Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 6, p. 1, doi. 10.1002/ajmg.b.32971
By:
- Forbes, Elana J.;
- Morison, Lottie D.;
- Lelik, Fatma;
- Howell, Tegan;
- Debono, Simone;
- Goel, Himanshu;
- Burger, Pauline;
- Mandel, Jean‐Louis;
- Geneviève, David;
- Amor, David J.;
- Morgan, Angela T.
Publication type:
Article
Low‐grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis‐like syndrome.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 6, p. 1, doi. 10.1002/ajmg.b.32976
By:
- Cogliati, Francesca;
- Straniero, Letizia;
- Rimoldi, Valeria;
- Masciadri, Maura;
- Perego, Sara;
- Rinaldi, Berardo;
- Milani, Donatella;
- Gentilini, Davide;
- Larizza, Lidia;
- Asselta, Rosanna;
- Russo, Silvia;
- Bedeschi, Maria Francesca
Publication type:
Article
FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 6, p. 1, doi. 10.1002/ajmg.b.32970
By:
- Mazel, Benoit;
- Delanne, Julian;
- Garde, Aurore;
- Racine, Caroline;
- Bruel, Ange‐Line;
- Duffourd, Yannis;
- Lopergolo, Diego;
- Santorelli, Filippo Maria;
- Marchi, Viviana;
- Pinto, Anna Maria;
- Mencarelli, Maria Antonietta;
- Canitano, Roberto;
- Valentino, Floriana;
- Papa, Filomena Tiziana;
- Fallerini, Chiara;
- Mari, Francesca;
- Renieri, Alessandra;
- Munnich, Arnold;
- Niclass, Tanguy;
- Le Guyader, Gwenaël
Publication type:
Article