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10
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mitochondrial dynamics and interorganellar communication in the development and dysmorphism of mammalian oocytes.[2019][j biochem].pdf
- JBSpecial Issue ReviewMitochondrialdynamics interorganellarcommunication inthe development mammalian
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11
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Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism.pdf
- Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism
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22
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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.pdf
- Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
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7
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the usefulness of reformatting ct scanning plane to distinguish sacral dysmorphism and introducing the variable of elevated height for predicting t.pdf
- the usefulness of reformatting ct scanning plane to distinguish sacral dysmorphism and introducing the variable of elevated height for predicting t
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2
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Stiffness, Facial Dysmorphism, and Skeletal Abnormalities Schwartz-Jampel Syndrome 1A.pdf
- Stiffness, Facial Dysmorphism, and Skeletal Abnormalities Schwartz-Jampel Syndrome 1A
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8
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Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay.pdf
- Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay
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4
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Antenatal Diagnosis of Jeune Syndrome (Asphyxiating Thoracic Dysplasia) with Micromelia and Facial Dysmorphism on Second-Trimester Ultrasound.pdf
- Antenatal Diagnosis of Jeune Syndrome (Asphyxiating Thoracic Dysplasia) with Micromelia and Facial Dysmorphism on Second-Trimester Ultrasound
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5
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A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism.pdf
- A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism
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4
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A filamin A splice mutation resulting in a syndrome of facial dysmorphism, periventricular nodular heterotopia, and severe constipation reminiscent of cerebro-fronto-facial syndrome.pdf
- A filamin A splice mutation resulting in a syndrome of facial dysmorphism, periventricular nodular heterotopia, and severe constipation reminiscent of cerebro‐fronto‐facial syndrome
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向豆丁求助：有没有dysmorphism?
