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Fig. 2 | Reproductive Biology and Endocrinology

Fig. 2

From: Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1

Fig. 2

Pedigree and sequencing results of families 4 and 5. A Pedigree and sequencing results of family 4. Sanger sequencing showed that the proband (II1) carried a heterozygous FGFR1 c.1835delA mutation, while the proband’s father (I1) and mother (I2) were normal. B Pedigree and CNV-seq results of family 5. CNV-seq results showed that the proband (II1) carried a 2.32 Mb deletion at 8p12-p11.22 (36,140,000–38,460,000), while the proband’s father (I1) and mother (I2) were normal

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Reproductive Biology and Endocrinology

ISSN: 1477-7827

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