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

Results: 8

1

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

2

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

3

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

4

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

5

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

6

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

7

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

8

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