Results
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2981.
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2982.
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2983.
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2984.
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2985.
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Exome sequencing in infants with congenital hearing impairment: a population-based cohort study. [electronic resource] by
- Downie, Lilian
- Halliday, Jane
- Burt, Rachel
- Lunke, Sebastian
- Lynch, Elly
- Martyn, Melissa
- Poulakis, Zeffie
- Gaff, Clara
- Sung, Valerie
- Wake, Melissa
- Hunter, Matthew F
- Saunders, Kerryn
- Rose, Elizabeth
- Lewis, Sharon
- Jarmolowicz, Anna
- Phelan, Dean
- Rehm, Heidi L
- Amor, David J
Producer: 20210525
In:
European journal of human genetics : EJHG vol. 28
Availability: No items available.
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2986.
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Neonatal Screening for Congenital Hypothyroidism: What Can We Learn From Discordant Twins? [electronic resource] by
- Medda, Emanuela
- Vigone, Maria Cristina
- Cassio, Alessandra
- Calaciura, Francesca
- Costa, Pietro
- Weber, Giovanna
- de Filippis, Tiziana
- Gelmini, Giulia
- Di Frenna, Marianna
- Caiulo, Silvana
- Ortolano, Rita
- Rotondi, Daniela
- Bartolucci, Monica
- Gelsomino, Rossella
- De Angelis, Simona
- Gabbianelli, Marco
- Persani, Luca
- Olivieri, Antonella
Producer: 20200604
In:
The Journal of clinical endocrinology and metabolism vol. 104
Availability: No items available.
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2987.
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2988.
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2989.
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Newborn screening of mucopolysaccharidoses: past, present, and future. [electronic resource] by
- Arunkumar, Nivethitha
- Langan, Thomas J
- Stapleton, Molly
- Kubaski, Francyne
- Mason, Robert W
- Singh, Rajendra
- Kobayashi, Hironori
- Yamaguchi, Seiji
- Suzuki, Yasuyuki
- Orii, Kenji
- Orii, Tadao
- Fukao, Toshiyuki
- Tomatsu, Shunji
Producer: 20210127
In:
Journal of human genetics vol. 65
Availability: No items available.
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2990.
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2991.
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2992.
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2995.
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2996.
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2997.
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2998.
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2999.
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3000.
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