M
Mary H. Puck
Researcher at Jewish Hospital
Publications - 5
Citations - 196
Mary H. Puck is an academic researcher from Jewish Hospital. The author has contributed to research in topics: Human chorionic gonadotropin & Klinefelter syndrome. The author has an hindex of 5, co-authored 5 publications receiving 190 citations. Previous affiliations of Mary H. Puck include University of Colorado Denver.
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Journal ArticleDOI
Pituitary-gonadal function in Klinefelter syndrome before and during puberty.
James A. Salbenblatt,James A. Salbenblatt,Bruce G. Bender,Bruce G. Bender,Mary H. Puck,Mary H. Puck,Arthur Robinson,Arthur Robinson,Charles Faiman,Jeremy S.D. Winter +9 more
TL;DR: Serum concentrations of follicle-stimulating hormone, luteinizing hormone, testosterone, and estradiol were determined at intervals before and during puberty in 40 individuals with Klinefelter syndrome (47,XXY karyotype), of whom 27 had been detected in neonatal cytogenetic screening programs.
Journal ArticleDOI
The development of four unselected 47,XYY boys.
Bruce G. Bender,Bruce G. Bender,Mary H. Puck,Mary H. Puck,James A. Salbenblatt,Arthur Robinson,Arthur Robinson +6 more
TL;DR: Four infants identified through neonatal screening programs are an unselected sample of 47,XYY boys, and all four demonstrated problems in motor and language development, leading to the hypothesis that their karyotype may heighten vulnerability to pre‐existing familial conditions.
Journal ArticleDOI
Short communication: skeletal maturation of children with sex chromosome abnormalities.
M. Lynn Webber,Mary H. Puck,Mary H. Puck,Marion M. Maresh,Walter B. Goad,Arthur Robinson,Arthur Robinson +6 more
TL;DR: This is the first documentation in a group of children with sex chromosome abnormalities, ascertained in an unbiased fashion, that, with the exception of those with a 45,X karyotype, bone age is not significantly different from that of the normal population.
Journal ArticleDOI
The meaning of early knowledge of a child's infertility in families with 47,XXY and 45,X children.
Joyce B. Borelli,Joyce B. Borelli,Bruce G. Bender,Bruce G. Bender,Mary H. Puck,Mary H. Puck,James A. Salbenblatt,James A. Salbenblatt,Arthur Robinson,Arthur Robinson +9 more
TL;DR: Nine girls with X or partial X monosomy and fourteen boys with 47,XXY karyotypes were identified through the consecutive chromosome screening of 40,000 newborns over a ten-year period, and the probable infertility of these children emerged as a central concern in psychiatric interviews with parents.
Journal ArticleDOI
Parents' adaptation to early diagnosis of sex chromosome anomalies
TL;DR: It was found that most achieved satisfactory understanding of the diagnosis with minimal disturbance, preferred early disclosure, denied its influence on parent-child and parent-parent relationships, and were reasonably comfortable in sharing diagnostic information with the child.